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Background and Aims: Monocyte chemotactic protein-1 (MCP-1) is a potent chemoattractant for monocytes. It is involved in pathogenesis of several inflammatory diseases. Hepatic MCP-1 is a readout of macrophage activation. While inflammation is a major driver of liver disease progression, the origin and role of circulating MCP-1 as a biomarker remains unclear.
Methods: Hepatic CC-chemokine ligand 2 (CCL2) expression and F4/80 staining for Kupffer cells were measured and correlated in a mouse model of chronic liver disease (inhalative CCl4 for 7 weeks). Next, hepatic RNA levels of CCL2 were measured in explanted livers of 39 patients after transplantation and correlated with severity of disease. Changes in MCP-1 were further evaluated in a rat model of experimental cirrhosis and acute-on-chronic liver failure (ACLF). Finally, we analyzed portal and hepatic vein levels of MCP-1 in patients receiving transjugular intrahepatic portosystemic shunt insertion for complications of portal hypertension.
Results: In this mouse model of fibrotic hepatitis, hepatic expression of CCL2 (P = 0.009) and the amount of F4/80 positive cells in the liver (P < 0.001) significantly increased after induction of hepatitis by CCl4 compared to control animals. Moreover, strong correlation of hepatic CCL2 expression and F4/80 positive cells were seen (P = 0.023). Furthermore, in human liver explants, hepatic transcription levels of CCL2 correlated with the MELD score of the patients, and thus disease severity (P = 0.007). The experimental model of ACLF in rats revealed significantly higher levels of MCP-1 plasma (P = 0.028) and correlation of hepatic CCL2 expression (R = 0.69, P = 0.003). Particularly, plasma MCP-1 levels did not correlate with peripheral blood monocyte CCL2 expression. Finally, higher levels of MCP-1 were observed in the hepatic compared to the portal vein (P = 0.01) in patients receiving TIPS. Similarly, a positive correlation of MCP-1 with Child-Pugh score was observed (P = 0.018). Further, in the presence of ACLF, portal and hepatic vein levels of MCP-1 were significantly higher compared to patients without ACLF (both P = 0.039).
Conclusion: Circulating levels of MCP-1 mainly derive from the injured liver and are associated with severity of liver disease. Therefore, liver macrophages contribute significantly to disease progression. Circulating MCP-1 may reflect the extent of hepatic macrophage activation.
Background: Point of care devices for performing targeted coagulation substitution in patients who are bleeding have become increasingly important in recent years. New on the market is the Quantra. It is a device that uses sonorheometry, a sonic estimation of elasticity via resonance, which is a novel ultrasound-based technology that measures viscoelastic properties of whole blood. Several studies have already shown the comparability of the Quantra with devices already established on the market, such as the rotational thromboelastometry (ROTEM) device.
Objective: In contrast to existing studies, this study is the first prospective interventional study using this new system in a cardiac surgical patient cohort. We will investigate the noninferiority between an already existing coagulation algorithm based on the ROTEM/Multiplate system and a new algorithm based on the Quantra system for the treatment of coagulopathic cardiac surgical patients.
Methods: The study is divided into two phases. In an initial observation phase, whole blood samples of 20 patients obtained at three defined time points (prior to surgery, after completion of cardiopulmonary bypass, and on arrival in the intensive care unit) will be analyzed using both the ROTEM/Multiplate and Quantra systems. The obtained threshold values will be used to develop a novel algorithm for hemotherapy. In a second intervention phase, the new algorithm will be tested for noninferiority against an algorithm used routinely for years in our department.
Results: The main objective of the examination is the cumulative loss of blood within 24 hours after surgery. Statistical calculations based on the literature and in-house data suggest that the new algorithm is not inferior if the difference in cumulative blood loss is <150 mL/24 hours.
Conclusions: Because of the comparability of the Quantra sonorheometry system with the ROTEM measurement methods, the existing hemotherapy treatment algorithm can be adapted to the Quantra device with proof of noninferiority.
Trial Registration: ClinicalTrials.gov NCT03902275; https://clinicaltrials.gov/ct2/show/NCT03902275
International Registered Report Identifier (IRRID): DERR1-10.2196/17206
Shares of open-end real estate funds are typically traded directly between the investor and the fund management company. However, we provide empirical evidence for the growth of secondary market activities, i.e., the trading of shares on stock exchanges. We find high trading levels in situations where the fund management company suspends the issue or redemption of shares. Shares trade at a discount when the fund management company suspends the redemption, whereas shares trade at a premium when the fund management company suspends the issue. We also find evidence that secondary market trading activity is increasing since German regulation introduced a minimum holding period and a mandatory notice period for open-end real estate funds.
Mobilität ist eine wesentliche Voraussetzung für soziale Teilhabe. Jedoch ist Mobilität mit Kosten verbunden, sodass die soziale Teilhabe bei geringen finanziellen Mitteln gefährdet sein kann. Das Projekt Social2Mobility begegnet dieser Problematik, indem es das Ziel verfolgt, die soziale Teilhabe von Menschen, die von finanzieller Armut betroffen oder bedroht sind, durch Stärkung ihrer Mobilität zu steigern. Um dieses Ziel zu erreichen, soll im Rahmen des Projektes in der Region Hannover ein Reallabor eingerichtet werden. Das Arbeitspapier begleitet dessen Konzeption und geht der Frage nach, inwiefern in der Region Hannover ein Reallabor zum Thema mobilitätsbezogene soziale Exklusion eingerichtet werden kann. So werden in diesem Arbeitspapier die konzeptionellen Überlegungen zur räumlichen Verortung, zur Zielgruppenauswahl und zu möglichen Themen für das Reallabor dargestellt. Zudem werden die Spezifizierung auf die Zielgruppen Haushalte mit Kindern und ältere Menschen (ab 60 Jahren) sowie die Auswahl der Kommune Ronnenberg als Verortung für das Reallabor begründet.
Using a dedicated data sample taken in 2018 on the J/ψ peak, we perform a detailed study of the trigger efficiencies of the BESIII detector. The efficiencies are determined from three representative physics processes, namely Bhabha scattering, dimuon production and generic hadronic events with charged particles. The combined efficiency of all active triggers approaches 100% in most cases, with uncertainties small enough not to affect most physics analyses.
Measurement of cross sections for e⁺e⁻ → μ⁺μ⁻ at center-of-mass energies from 3.80 to 4.60 GeV
(2020)
The observed cross sections for 𝑒+𝑒−→𝜇+𝜇− at energies from 3.8 to 4.6 GeV are measured using data samples taken with the BESIII detector operated at the BEPCII collider. We measure the muonic widths and determine the branching fractions of the charmonium states 𝜓(4040), 𝜓(4160), and 𝜓(4415) decaying to 𝜇+𝜇−, as well as making a first determination of the phase of the amplitudes. In addition, we observe evidence for a structure in the dimuon cross section near 4.220 GeV/𝑐2, which we denote as 𝑆(4220). Analyzing a coherent sum of amplitudes yields eight solutions, one of which gives a mass of 𝑀𝑆(4220) = 4216.7±8.9±4.1 MeV/𝑐2, a total width of Γtot S(4220) = 47.2±22.8±10.5 MeV, and a muonic width of Γ𝜇𝜇 𝑆(4220) = 1.53±1.26±0.54 keV, where the first uncertainties are statistical and the second systematic. The eight solutions give the central values of the mass, total width, muonic width to be, respectively, in the range from 4212.8 to 4219.4 MeV/𝑐2, from 36.4 to 49.6 MeV, and from 1.09 to 1.53 keV. The statistical significance of the 𝑆(4220) signal is 3.9𝜎. Correcting the total dimuon cross section for radiative effects yields a statistical significance for this structure of 8.1𝜎.
Using 2.93 fb−1 of 𝑒+𝑒− collision data collected at a center-of-mass energy of 3.773 GeV with the BESIII detector, the first observation of the doubly Cabibbo-suppressed decay 𝐷+→𝐾+𝜋+𝜋−𝜋0 is reported. After removing decays that contain narrow intermediate resonances, including 𝐷+→𝐾+𝜂, 𝐷+→𝐾+𝜔, and 𝐷+→𝐾+𝜙, the branching fraction of the decay 𝐷+→𝐾+𝜋+𝜋−𝜋0 is measured to be (1.13±0.08stat±0.03syst)×10−3. The ratio of branching fractions of 𝐷+→𝐾+𝜋+𝜋−𝜋0 over 𝐷+→𝐾−𝜋+𝜋+𝜋0 is found to be (1.81±0.15)%, which corresponds to (6.28±0.52)tan4𝜃𝐶, where 𝜃𝐶 is the Cabibbo mixing angle. This ratio is significantly larger than the corresponding ratios for other doubly Cabibbo-suppressed decays. The asymmetry of the branching fractions of charge-conjugated decays 𝐷±→𝐾±𝜋±𝜋∓𝜋0 is also determined, and no evidence for 𝐶𝑃 violation is found. In addition, the first evidence for the 𝐷+→𝐾+𝜔 decay, with a statistical significance of 3.3𝜎, is presented and the branching fraction is measured to be ℬ(𝐷+→𝐾+𝜔) = (5.7+2.5−2.1stat±0.2syst)×10−5.
Using a sample of 106 million 𝜓(3686) decays, 𝜓(3686)→𝛾𝜒𝑐𝐽(𝐽=0,1,2) and 𝜓(3686)→𝛾𝜒𝑐𝐽,𝜒𝑐𝐽→𝛾𝐽/𝜓(𝐽=1,2) events are utilized to study inclusive 𝜒𝑐𝐽→anything, 𝜒𝑐𝐽→hadrons, and 𝐽/𝜓→anything distributions, including distributions of the number of charged tracks, electromagnetic calorimeter showers, and 𝜋0s, and to compare them with distributions obtained from the BESIII Monte Carlo simulation. Information from each Monte Carlo simulated decay event is used to construct matrices connecting the detected distributions to the input predetection “produced” distributions. Assuming these matrices also apply to data, they are used to predict the analogous produced distributions of the decay events. Using these, the charged particle multiplicities are compared with results from MARK I. Further, comparison of the distributions of the number of photons in data with those in Monte Carlo simulation indicates that G-parity conservation should be taken into consideration in the simulation.
The processes 𝑒+𝑒−→𝐷+ 𝑠𝐷𝑠1(2460)−+c.c. and 𝑒+𝑒−→𝐷*+ 𝑠𝐷𝑠1(2460)−+c.c. are studied for the first time using data samples collected with the BESIII detector at the BEPCII collider. The Born cross sections of 𝑒+𝑒−→𝐷+ 𝑠𝐷𝑠1(2460)−+c.c. at nine center-of-mass energies between 4.467 GeV and 4.600 GeV and those of 𝑒+𝑒−→𝐷*+ 𝑠𝐷𝑠1(2460)−+c.c. at √𝑠=4.590 GeV and 4.600 GeV are measured. No obvious charmonium or charmoniumlike structure is seen in the measured cross sections.
We examined the feedback between the major protein degradation pathway, the ubiquitin-proteasome system (UPS), and protein synthesis in rat and mouse neurons. When protein degradation was inhibited, we observed a coordinate dramatic reduction in nascent protein synthesis in neuronal cell bodies and dendrites. The mechanism for translation inhibition involved the phosphorylation of eIF2α, surprisingly mediated by eIF2α kinase 1, or heme-regulated kinase inhibitor (HRI). Under basal conditions, neuronal expression of HRI is barely detectable. Following proteasome inhibition, HRI protein levels increase owing to stabilization of HRI and enhanced translation, likely via the increased availability of tRNAs for its rare codons. Once expressed, HRI is constitutively active in neurons because endogenous heme levels are so low; HRI activity results in eIF2α phosphorylation and the resulting inhibition of translation. These data demonstrate a novel role for neuronal HRI that senses and responds to compromised function of the proteasome to restore proteostasis.
Protein turnover, the net result of protein synthesis and degradation, enables cells to remodel their proteomes in response to internal and external cues. Previously, we analyzed protein turnover rates in cultured brain cells under basal neuronal activity and found that protein turnover is influenced by subcellular localization, protein function, complex association, cell type of origin, and by the cellular environment (Dörrbaum et al., 2018). Here, we advanced our experimental approach to quantify changes in protein synthesis and degradation, as well as the resulting changes in protein turnover or abundance in rat primary hippocampal cultures during homeostatic scaling. Our data demonstrate that a large fraction of the neuronal proteome shows changes in protein synthesis and/or degradation during homeostatic up- and down-scaling. More than half of the quantified synaptic proteins were regulated, including pre- as well as postsynaptic proteins with diverse molecular functions.
Selbstübersetzungen sind faszinierende Erscheinungsformen mehr- und anderssprachigen Schreibens. Sie bewegen sich an der Grenze zwischen pragmatischem Nutzen und autorschaftlicher Strategie, sie eröffnen die Lizenz zum produktiven Weiterdenken, Umstellen und Fortsetzen des Ausgangstextes, und oft werfen sie die Frage auf, welche der so entstehenden Versionen das Original und welche die Übersetzung ist. Bisherige Untersuchungen zum Thema konzentrierten sich meist auf literarische, insbesondere poetische Selbstübersetzungen. Der vorliegende Band nimmt dagegen das Moment der Übertragung von Wissen in den Blick - und damit den spannungsvollen Zusammenhang von sprachlichem Transfer und Wissenstransfer. Die Beiträge widmen sich gelehrten und intellektuellen Selbstübersetzern aus fünf Jahrhunderten: Martin Luther, Jan Baptista van Helmont, August Wilhelm Schlegel, Wilhelm und Alexander von Humboldt, Alessandro Manzoni, Heinrich Heine, Leo Spitzer, Walter Benjamin, Kurt Goldstein, Eugen Rosenstock-Huessy, Cornelius Castoriadis, Humberto Maturana und Wolfgang Iser.
Selbstübersetzung - das heißt: Autorinnen und Autoren übertragen ihre eigenen Texte aus einer Sprache in eine andere Sprache, fungieren also als ihre eigenen Übersetzerinnen und Übersetzer. In einer Selbstübersetzung sind demnach Autor und Übersetzer identisch. Aus dieser vermeintlich einfachen Definition ergibt sich eine Reihe von komplexen Forschungsfragen. Sie lassen sich anhand einiger Leitbegriffe formulieren, um das im vorliegenden Band unternommene Gespräch über die Grenzen von Philologien und Disziplinen hinweg ansatzweise zu systematisieren.
Cross sections of the process 𝑒+𝑒−→𝜋0𝜋0𝐽/𝜓 at center-of-mass energies between 3.808 and 4.600 GeV are measured with high precision by using 12.4 fb−1 of data samples collected with the BESIII detector operating at the BEPCII collider facility. A fit to the measured energy-dependent cross sections confirms the existence of the charmoniumlike state 𝑌(4220). The mass and width of the 𝑌(4220) are determined to be (4220.4±2.4±2.3) MeV/𝑐2 and (46.2±4.7±2.1) MeV, respectively, where the first uncertainties are statistical and the second systematic. The mass and width are consistent with those measured in the process 𝑒+𝑒−→𝜋+𝜋−𝐽/𝜓. The neutral charmonium-like state 𝑍𝑐(3900)0 is observed prominently in the 𝜋0𝐽/𝜓 invariant-mass spectrum, and, for the first time, an amplitude analysis is performed to study its properties. The spin-parity of 𝑍𝑐(3900)0 is determined to be 𝐽𝑃=1+, and the pole position is (3893.1±2.2±3.0)−𝑖(22.2±2.6±7.0) MeV/𝑐2, which is consistent with previous studies of electrically charged 𝑍𝑐(3900)±. In addition, cross sections of 𝑒+𝑒− → 𝜋0𝑍𝑐(3900)0 → 𝜋0𝜋0𝐽/𝜓 are extracted, and the corresponding line shape is found to agree with that of the 𝑌(4220).
The process 𝑒+𝑒−→𝜙𝜂′ has been studied for the first time in detail using data sample collected with the BESIII detector at the BEPCII collider at center of mass energies from 2.05 to 3.08 GeV. A resonance with quantum numbers 𝐽𝑃𝐶=1−− is observed with mass 𝑀=(2177.5±4.8(stat)±19.5(syst))MeV/𝑐2 and width Γ=(149.0±15.6(stat)±8.9(syst)) MeV with a statistical significance larger than 10𝜎, including systematic uncertainties. If the observed structure is identified with the 𝜙(2170), then the ratio of partial width between the 𝜙𝜂′ by BESIII and 𝜙𝜂 by BABAR is (ℬ𝑅𝜙𝜂Γ𝑅𝑒𝑒)/(ℬ𝑅𝜙𝜂′Γ𝑅𝑒𝑒)=0.23±0.10(stat)±0.18(syst), which is smaller than the prediction of the 𝑠¯𝑠𝑔 hybrid models by several orders of magnitude.
By analyzing a data sample corresponding to an integrated luminosity of 2.93 fb−1 collected at a center-of-mass energy of 3.773 GeV with By analyzing a data sample corresponding to an integrated luminosity of 2.93 fb−1 collected at a center-of-mass energy of 3.773 GeV with the BESIII detector, we measure for the first time the absolute branching fraction of the 𝐷+→𝜂𝜇+𝜈𝜇 decay to be ℬ𝐷+→𝜂𝜇+𝜈𝜇=(10.4±1.0stat±0.5syst)×10−4. Using the world averaged value of ℬ𝐷+→𝜂𝑒+𝜈𝑒, the ratio of the two branching fractions is determined to be ℬ𝐷+→𝜂𝜇+𝜈𝜇/ℬ𝐷+→𝜂𝑒+𝜈𝑒=0.91±0.13(stat+syst), which agrees with the theoretical expectation of lepton flavor universality within uncertainty. By studying the differential decay rates in five four-momentum transfer intervals, we obtain the product of the hadronic form factor 𝑓𝜂+(0) and the 𝑐→𝑑 Cabibbo-Kobayashi-Maskawa matrix element |𝑉𝑐𝑑| to be 𝑓𝜂+(0)|𝑉𝑐𝑑|=0.087±0.008stat±0.002syst. Taking the input of |𝑉𝑐𝑑| from the global fit in the standard model, we determine 𝑓𝜂+(0)=0.39±0.04stat±0.01syst. On the other hand, using the value of 𝑓𝜂+(0) calculated in theory, we find |𝑉𝑐𝑑| = 0.242±0.022stat±0.006syst±0.033theory.
We report the first observation of the semimuonic decay 𝐷+→𝜔𝜇+𝜈𝜇 using an 𝑒+𝑒− collision data sample corresponding to an integrated luminosity of 2.93 fb−1 collected with the BESIII detector at a center-of-mass energy of 3.773 GeV. The absolute branching fraction of the 𝐷+→𝜔𝜇+𝜈𝜇 decay is measured to be ℬ𝐷+→𝜔𝜇+𝜈𝜇=(17.7±1.8stat±1.1syst)×10−4. Its ratio with the world average value of the branching fraction of the 𝐷+→𝜔𝑒+𝜈𝑒 decay probes lepton flavor universality and it is determined to be ℬ𝐷+→𝜔𝜇+𝜈𝜇/ℬPDG 𝐷+→𝜔𝑒+𝜈𝑒=1.05±0.14, in agreement with the standard model expectation within one standard deviation.
Die maßgebliche Position des Übersetzungskonzepts ergibt nicht nur aus dem unweigerlich vielsprachigen, migrierenden und interdisziplinären Denken des Philosophen, Psychoanalytikers, Ökonomen und Aktivisten Cornelius Castoriadis. Vielmehr existiert ein konkreter Kern des Translatorischen in den zwei konstitutiven Gegenständen seiner Philosophie, im Imaginären einerseits und anderseits in der Politik, die auf die imaginäre Verfasstheit der Gesellschaft zurückgeht. Ob also Castoriadis seinen eigenen Text vom Französischen in die griechische Sprache überträgt oder ob er die Vorstellungswelt der kapitalistischen Gegenwart beschreibt - in beiden Fällen geht es um die Übersetzung als einen kreativen Prozess innerhalb der Sprache, des Denkens oder der Politik.
Anhand des wissenschaftsphilosophischen Sachbuches "Der Baum der Erkenntnis" ("El árbol del conocimiento"), das in den 1980er Jahren von den chilenischen Biologen und Neurowissenschaftlern Humberto Maturana und Francisco Varela in spanischer Sprache veröffentlich wurde und für den Soziologen Niklas Luhmann zu einem wichtigen Standbein seiner Theorie der Gesellschaft und der sozialen Systeme wurde, soll gezeigt werden, wie einerseits Selbstübersetzung von der Wissenschaft in die Öffentlichkeit und andererseits Fremdübersetzung von der einen Sprache in die andere - in diesem Fall aus dem Spanischen ins Deutsche und Englische - Interferenzen und Reibungen innerhalb des Wissenstransfers produzieren. Zunächst soll ein Überblick über die unterschiedlichen Formen des Popularisierens als interdiskursive Selbstübersetzung gegeben werden. Im zweiten Teil wird dann die interlinguale Übersetzungsleistung diskutiert, die das spanische Original durch jeweils andere Sprach- und Forschungskontexte leicht verändert und dem fremdsprachigen Begriffsrepertoire einverleibt. Zuletzt soll in einem dritten Teil mit Rückgriff auf Luhmann das Prinzip der Autopoiesis als ein Prozess ausgewiesen werden, der bereits in "El árbol del conocimiento" nicht einfach als ein Wissenstransfer zu verstehen ist, sondern als ein Transfer der Bedingungen, wie Wissen im Übersetzen vom Übersetzen entsteht.
This article takes the renowned study "Der Akt des Lesens" (1976) by Wolfgang Iser and its translation "The Act of Reading" (1978) as its starting point. The differences between the two texts are discussed in terms of Iser's own idea of translatability as a cultural practice that was outlined in the short text "On Translatability". This theoretical frame will shed light on the decisions made in his own translations, and will help to develop a conceptualization of self-translation as a practice inherent in cultural change. [...] I will propose a combination of two concepts, Iser's 'translatability' (in II.) and the notion of 'autocommunication' by Lotman (III.), to suggest a concept of self-translation that entails three interrelated aspects: a) translation as a rewriting of the text as such, b) translation as continued work on one's argument as well as c) the re-translation back to the original source as a manifestation of a change in one's thought structure - Änderungen der eigenen Denkstruktur, as one of Werner Heisenberg's papers is entitled, and to which I will come back in my conclusion (IV.). Hence, the focus is mainly systematic and conceptual, however, I will first comment on my example of self- and re-translation and start with a comparison of different versions of Iser's "Der Akt des Lesens" and the shorter texts that led to the actual monograph.
Die komplexe und diffizile Frage, der im vorliegenden Beitrag nachgegangen werden soll, ist die nach Heines Eigenschaft als Selbstübersetzer, womit das Hauptaugenmerk auf die sprachlichen d. h. mehrsprachigen Grundlagen seiner Vermittlungstätigkeit gerichtet wird. Denn die Bezeichnung Heines als Selbstübersetzer kann im Gegensatz zur Assoziierung mit dem Begriff des Kulturtransfers durchaus überraschen. Mit Heines Sprachkompetenz im Französischen und dem auktorialen Status seiner französischen Schriften werden Forschungsfragen berührt, die in der Heine-Kritik von ihren Anfängen bis heute durchaus kontrovers diskutiert werden. In diesem Zusammenhang wäre auch nachzudenken über den für die Analyse von Heines Schreib- und Veröffentlichungspraxis relevanten Begriff von Übersetzung bzw. Selbstübersetzung. Kann man im Falle Heines wirklich von einem alleinigen deutschen Original sprechen und den französischen Fassungen seiner Schriften - wie oft geschehen - einen bloß sekundären Status zuweisen? In diesem Problemzusammenhang spielt neben den textgenetischen und sprachlich-translatorischen Aspekten auch die Perspektive der Selbstdarstellung bzw. Selbstvermarktung des Dichters eine bedeutende Rolle, insofern man bei Heine von einer regelrechten Inszenierung als zweisprachigem Autor reden kann. Die von mir im Folgenden vertretene These wird hierbei lauten, dass Heinrich Heines durchaus fragwürdiger Status als Selbstübersetzer über normative Übersetzungs- und Sprachkompetenzkriterien hinaus vor allem als doppelte - d. h. binationale und zweisprachige - 'auctoritas' aufzufassen ist. Anders gesagt: Über die komplexe Frage der Textgenese hinaus soll die von Heine bewusst eingenommene Rolle als direkter Akteur zweier nationaler Wissenssysteme betont werden. Unter diesem Blickwinkel wird nicht zuletzt ein bemerkenswerter Nexus zwischen den vermittelten Wissensinhalten und deren sprachlichem Transfer sichtbar. So soll gezeigt werden, dass Heines dezidiert antinationalistisches, kosmopolitisches und universalistisches Denken zwischen Deutschland und Frankreich seine formale Entsprechung in einer interlingualen Wissenszirkulation zwischen der deutschen und der französischen Sprache findet, in deren Medium die von ihm entwickelten und vermittelten Theorien und Thesen prozessual entwickelt und weitergeschrieben werden. Eine solche Sichtweise auf Heine als translingualen Schriftsteller wurde bisher nicht immer ausreichend von der Forschung berücksichtigt und gewürdigt. Wie allgemein im Zusammenhang mit bikulturellen und bilingualen Autoren sowie sprachlich hybriden Schreibverfahren wird man mit blinden Flecken der Forschung und nationalphilologischen Widerständen konfrontiert, die eine mehr oder weniger symbolische 'Vereinsprachigung' von Heines Werken befördern oder implizieren. Dieser Umstand betrifft nicht nur die deutsche Heine-Rezeption, sondern ist bedauerlicherweise auch in der interkulturell aufgestellten französischen Germanistik der jüngeren Zeit zu beobachten, wie ich in einem abschließenden Exkurs zeigen möchte.
Auf der harten Schulbank der Sprache : Leo Spitzers Bemerkungen über das Erlernen des Türkischen
(2020)
Im Folgenden werde ich mich mit einem Aufsatz von Leo Spitzer befassen, der als sonderbarer Fall von Selbstübersetzung rezipiert wurde. Dieser Text, in dem er seine persönlichen Erfahrungen mit dem Erwerb des Türkischen reflektiert und anschließend aus semantisch vergleichender Perspektive die türkische Syntax untersucht, wurde beinahe zeitgleich in einer französischen und einer türkischen Fassung veröffentlicht. Im Jahre 1935 erschien die französische Fassung des Aufsatzes über das Türkischlernen im Bulletin de la Société de linguistique de Paris: "En apprenant le turc. (Considérations psychologiques sur cette langue)" (wörtlich: "Türkisch lernend. Psychologische Betrachtungen über diese Sprache"). Im gleichen Zeitraum, sogar etwas früher, erschien auch eine türkische Fassung des Beitrags unter dem Titel "Türkçeyi Öğrenirken" ("Türkisch lernend") - ohne Untertitel -, die in drei Teilen in der literarischen Zeitschrift Varlık (Das Sein) zwischen April 1934 und Januar 1935 veröffentlicht wurde. Interessanterweise scheint Spitzer den ersten Teil der türkischen Version selbst übersetzt oder direkt auf Türkisch verfasst zu haben. Die Übersetzung der beiden weiteren Teile wurde hingegen von seinem damaligen Assistenten Sabahattin Eyüboğlu (1908−1973) vorgenommen, der an der Übersetzungspolitik der Türkei in den dreißiger Jahren aktiv mitwirkte. Mit diesem Aufsatz bekommt die Frage nach sprach- bzw. wissenschaftspolitischem Wissenstransfer in Istanbul einen sonderbaren, ja karnevalistischen Gehalt: Ein Professor, der beauftragt wurde, die abendländische Philologie und Wissenskultur in die moderne Türkei einzuführen, zeigt sich selbst in der Haltung des Lernenden, der ein sprachwissenschaftliches Selbstexperiment wagt. Dadurch wird die Wahl der Sprache als Werkzeug der Wissensvermittlung infrage gestellt: Französisch und Türkisch, beides erlernte und dadurch vergleichbare Sprachen, die in diesem Aufsatz zugleich Gegenstand und Mittel der Stilforschung sind. Meine Überlegungen zu diesem Thema gliedern sich in drei aufeinander aufbauende Teile. Nach einer knappen Hinführung zu Leo Spitzers Sprachauffassung und seinem Verständnis von Sprachwissenschaft als Stilforschung werde ich die historische Situation seines Aufenthalts in Istanbul in den Jahren von 1933 bis 1936 umreißen. In einem zweiten Schritt werde ich den besagten Aufsatz genauer in Hinblick auf Fragen der Selbstübersetzung untersuchen und fragen, was Leo Spitzer motiviert hat, diese angebliche Selbstübersetzung vorzunehmen. Weder war er Turkologe noch hat er seine romanistischen Arbeiten selbst ins Türkische übersetzt: Die philologischen Forschungen, die er während des Exils in Istanbul unternommen hat, sind entweder auf Französisch oder auf Deutsch erschienen. Die Bedeutung der Entscheidung, speziell diesen Aufsatz über die türkische Sprache selbst zu 'übersetzen', möchte ich zuletzt angesichts der wissenschaftspolitischen Rivalität von Sprachen - in diesem Fall zwischen dem Französischen und dem Türkischen - beleuchten.
Für Walter Benjamin war das Übersetzen nicht zuletzt eine Lebenserfahrung. Spätestens seit 1933, also seitdem er als Exilant in Paris lebte, war das Oszillieren zwischen dem Deutschen und dem Französischen sein täglich Brot. Von den Herausforderungen, Spannungen und Aporien dieses permanenten Changierens zeugen in seinem Werk vor allem die Selbstübersetzungen. Denn Benjamin hat - was in der Forschung erstaunlich selten beachtet wird - zahlreiche Selbstübersetzungen aus dem Deutschen ins Französische angefertigt. [...] Das Exposé zum "Passagenwerk" hat Benjamin 1935 auf Deutsch unter dem Titel "Paris, die Hauptstadt des XIX. Jahrhunderts" verfasst und 1939 unter dem Titel "Paris, Capitale du XIXème siècle: Exposé" selbst ins Französische übersetzt. Um diese Schrift in ihrer deutschen und ihrer französischen Fassung geht es in meinem folgenden Beitrag. Ich möchte eine vergleichende Lektüre der beiden Exposés vorschlagen. In der Passage vom deutschen Ausgangstext zum französischen Text der Selbstübersetzung verändert sich, wie sich zeigen wird, die Form der Darstellung wie auch die Art der Argumentation auf signifikante Weise: Wir können in Benjamins Selbstübersetzung des Passagenexposés nachvollziehen, wie das Deutsche und das Französische in eine Konstellation treten und dennoch in keiner Weise ineinander aufgehen, da Fremdheit und Differenz das Paradigma der Übersetzung darstellen, wie übrigens auch im Zusammenhang mit Benjamins früher Übersetzungstheorie deutlich werden wird. Dies ist im Fall der Selbstübersetzung umso erstaunlicher, da es sich hier um ein vermeintlich identisches Autorsubjekt handelt. Die Selbstübersetzung stellt somit einen Fall der Übersetzung dar, in dem sich die Voraussetzungen der Benjamin'schen Übersetzungstheorie auf exemplarische Weise kristallisieren. Bevor ich eingehender auf die beiden Exposés und auf die Form der Selbstübersetzung zu sprechen komme, möchte ich deshalb einige sehr kurze allgemeine Überlegungen zum Verhältnis von Übersetzungstheorie und ‑praxis bei Walter Benjamin vorausschicken und sodann die beiden Exposés - das deutsche Original von 1935 und die Selbstübersetzung ins Französische von 1939 - kurz vorstellen und (werk‑)historisch einordnen. Vor diesem Hintergrund können und sollen dann einige Beobachtungen zu den beiden Exposés en détail diskutiert werden.
Goldsteins Karriere in den USA startete mit wichtigen Publikationen in der neuen Sprache und vollzog sich nahezu vollständig in der Fremdsprache, deutsche Aufsätze verzeichnet seine Bibliographie nach seiner Emigration nur ganz vereinzelt. [...] Auf der Ebene des bibliographischen Befundes handelte es sich also um einen nahezu vollständigen Übergang in die fremde Sprache unter bruchlos fortlaufender Publikationstätigkeit, an dessen Nahtstelle die Übersetzung seines wichtigsten Buches stand. [...] Aus der "Einführung in die Biologie unter besonderer Berücksichtigung der Erfahrungen am kranken Menschen" war "A Holistic Approach to Biology Derived from Pathological Data in Man" geworden. Das amerikanische Buch war keine 'Einführung' mehr, keine 'Introduction', sondern bereits der Untertitel signalisierte eine besondere Perspektive auf die Biologie. [...] Dabei liegt Goldsteins Originalität darin - so der erste Teil der These, die in diesem Aufsatz aus dem Vergleich des deutschen Originals mit der englischen Übersetzung entwickelt werden soll -, dass er aus seinen akribischen empirischen Beobachtungen eine neue epistemologische Perspektive auf organismische Prozesse entwickelt hat, mit der er zugleich die alten ontologischen Diskussionen um eine den Lebensphänomenen und den lebenden Systemen eigene Wesenheit überwunden zu haben hoffte. Genau diese Stoßrichtung verschleiert aber der entscheidende Zusatz zur englischen Übersetzung, wenn sie diesen 'approach' als 'holistisch' charakterisiert. Denn Holismus und Ganzheitlichkeit stehen typischerweise für jene ontologische Richtung des Vitalismus, gegen die sich Goldstein wiederholt explizit gewandt und die im Buch vor allem als Kritik an Hans Drieschs Entelechie-Lehre ihre Spuren hinterlassen hatte. Goldsteins epistemologische Neuausrichtung der Biologie hatte auch hinter seiner Distanz zur Psychoanalyse gestanden - bzw. sie theoretisch legitimiert, weil er wie viele seiner neuropsychiatrischen Kollegen die Verabsolutierung sexueller Motive seitens der Psychoanalyse nicht mitvollziehen wollte. 'Triebe' oder 'Instinkte' konnten als empirische Beschreibungen biologischer Verhaltensweisen durchaus ihre Zwecke erfüllen, aber wenn daraus eigene Entitäten wurden, war damit der Schritt von der Epistemologie zur Ontologie vollzogen, den Goldstein zu vermeiden suchte, weil seine Theorie des Organismus gerade auf die Differenz zwischen beiden wissenschaftlichen Perspektiven abhob. Der zweite Teil der These lautet deshalb, dass die englische Übersetzung von Goldsteins Buch maßgeblich seine Rezeption als holistischer Biophilosoph und damit als ontologischer Vitalist gebahnt hat. Diese entscheidende Verschiebung, die eigentlich im Widerspruch zur Präzisierung von 'Einführung' durch 'approach' steht, wurde vom Haupttitel noch verstärkt, weil hier gerade umgekehrt die epistemologische Perspektive fallengelassen wurde, die dem - zugegebenermaßen unübersetzbaren - Wort 'Aufbau' eingeschrieben war, während das selbstständig gewordene Wort 'Organismus' nun in der Tat eine Erörterung seines Wesens anzukündigen schien. [...] Vor dem Hintergrund der Entwicklung von Goldsteins Anschauungen erscheint die englische Übersetzung des Organismus-Buchs als Wendepunkt von einer Vitalismus-skeptischen und epistemologischen Form der Biophilosophie zu einer affirmativ-vitalistischen, ontologischen Position.
Seit Jacob Burckhardts Thesen zum Individualismus in der Renaissance gilt das 'Selbst' als eine eingehend diskutierte Größe, die ungeachtet ihrer diversen Erscheinungsformen nicht nur als das bündige Kennzeichen einer Schwellenzeit, sondern geradezu als ihr alleiniges Produkt angesehen wurde: die Epoche zwischen Spätmittelalter und Aufklärung steht schlichtweg für den 'Ursprung' der modernen Individualität. [...] Dem wohl prominentesten oratorischen Initiator, der explizit für eine 'reformatio mundi' steht, widerfuhr seitens der historiographischen Nachwelt bezeichnenderweise beides, eine ergebene Verklärung als Führergestalt sowie die Apotheose im prometheischen Schema: Martin Luther gilt bis heute nicht nur als 'Rebell' oder 'Revolutionär', sondern vor allem auch als 'Schöpfer der deutschen Schriftsprache'. Spätestens hier gilt es zu differenzieren. Gerade die Person des Wittenberger Gelehrten, Predigers und Seelsorgers gibt Anlass zur sorgsamen Klärung eines frühneuzeitlichen Selbst-Bewusstseins. Das Selbst-Verständnis des Augustinermönchs gründet zunächst ausschließlich in theologischen Traditionen und ist daher vor allem mit Komposita wie 'Selbsterforschung', 'Selbstgespräch' ('soliloquium') und 'Selbsterkenntnis' ('cognitio sui') in Verbindung zu bringen. Diese Kategorien aber sind primär und unlösbar an die Sündhaftigkeit jedes einzelnen Menschen gekoppelt [...] Und dennoch - in diesem der Moderne eher fremd anmutenden Katalog der genannten Komposita begegnet tatsächlich auch die 'SelbstÜbersetzung': als Praxis und Phänomen wie in Form erhellender Paraphrasierungen. Voraussetzung für die Praxis scheint zunächst ein Geschehen auf der machtpolitischen Ebene zu sein. Mit dem Rückgang der von Papst und Kaiser getragenen Universalherrschaft im westlichen Europa, mit dem Schwinden eines nachantiken Herrschaftsanspruchs ('translatio imperii') im Sinne des mittelalterlichen römischen Reichsgedankens ist gleichermaßen auch der rasch fortschreitende Rückgang des Lateinischen als flächendeckende Gelehrten- und Verwaltungssprache eingeleitet. Indem nun die einzelnen regionalen Teilherrschaften nach politischer Autonomie streben, erhält auch die polyphone Sprachkultur Europas einen neuen Stellenwert: weitgehend noch pränationale, also eher territoriale Interessenkollektive verlegen sich auf die Regelung ihrer Angelegenheiten im eigenen Idiom. Dieses kann damit aus dem Schattendasein eines als 'laienhaft' und 'illiterat' verachteten Ungenügens heraustreten und sich als vollgültiges Pendant der antiken Vorgaben erweisen. [...] Ein zweites Novum tritt zeitgleich hinzu. Zwecks parteigebundener Regelung der lokalen und bald auch der bi- oder multilateralen Angelegenheiten erhalten die antiken Vorgaben der Redekunst eine neue und sehr zentrale Funktion: das vor Ort im Sinne bestimmter Interessen auftretende Einzel- oder Kollektivsubjekt (Territorialgewalt) artikuliert sich sprachlich-persuasiv, vertritt einen lokalen Standpunkt ('opinio' / 'point de vue') und versucht seine Zuhörer durch Überzeugung zu einem politisch wirksamen Handeln zu bewegen. Hierfür dient der Autortext, ebenso aber auch seine zweckgerichtete Übersetzung. In dieser konkretisiert sich ein Subjekt nicht nur als Mittler zwischen Parteien, Ständen und Interessen, sondern auch zwischen Sprachen und Kulturen.
In the first half of this article I will explore Van Helmont's philosophy of language and translation, in part by contextualizing it within the sixteenth- and seventeenth-century traditions upon which he drew. Since Van Helmont is so explicit about the philosophy of language and translation that he developed, I will investigate in this article if he turned his philosophy into practice. Therefore, the second half of this article will discuss Van Helmont's practices of using and translating between his two main languages (Dutch and Latin). The way in which he employed the languages in which he wrote raises questions about his practice of self-translation and the use of language. Did his mother tongue always figure as the first language into which his thoughts were translated, or could it also have been Latin as the first language for his profession? Van Helmont might have been switching primary languages for the different purposes of his writings. Before going into more detail about his philosophy and use of language, I will briefly introduce this relatively unknown author to the reader.
Zwar verfasste und veröffentlichte Schlegel das Gros seiner Schriften auf Deutsch, mehrere wichtige Publikationen erschienen aber auf Französisch und Latein. Schlegels berühmte Übersetzungsleistungen und seine mehrsprachige Publikationspraxis legen die Vermutung nahe, er habe sich als Selbstübersetzer betätigt, um etwa seine deutschsprachigen Schriften für ein internationales Publikum zugänglich zu machen. Dies ist jedoch nicht der Fall: Entweder wurden seine Schriften von Dritten übersetzt, mit oder ohne Mitwirkung des Autors, oder er selbst hat die jeweilige Schrift direkt in der Fremdsprache verfasst. Diese Sprachwahl ist meines Erachtens ein wesentlicher Grundzug von Schlegels Publikationsstrategie. Schlegel übersetzte seine Schriften weder selbst noch gab er sie als Selbstübersetzungen an. Und trotzdem lässt sich bei Schlegel das Phänomen der Selbstübersetzung feststellen. Denn er übernahm frühere Gedanken, Ausdrücke und Botschaften in neue, in einer anderen Sprache verfasste Schriften und passte sie dem Zielpublikum an. So tauchen äquivalente Textpassagen, seien es einzelne Sätze, seien es ganze Absätze, in Texten auf, die in unterschiedlichen Sprachen verfasst wurden. Diese Selbstübersetzungen spiegeln auf einer interlingualen Ebene die enge intertextuelle Vernetzung seines scheinbar disparaten Werks wider und sind eng mit analogen intralingualen Verfahren wie Kommentieren, Paraphrasieren, Zusammenfassen oder Zitieren verbunden, die Schlegels Schreib- und Arbeitsweise prägen. Seine Texte zeichnen sich durch eine starke Selbstreferenz aus, die über die häufig vorkommenden und selten ausgewiesenen Selbstzitate sowie die Übernahme und Weiterentwicklung bereits an anderer Stelle ausformulierter Gedanken hinausgeht. Zunächst soll Schlegels selbstreferentielle Schreibweise anhand eines kurzen zweisprachigen Textvergleichs veranschaulicht werden (I.). Anschließend wird im Hauptteil dieses Beitrags (II.) Schlegels Selbstübersetzung anhand der "Comparaison entre la Phèdre de Racine et celle d'Euripide" und der Wiener Vorlesungen "Über dramatische Kunst und Literatur" beleuchtet. In einem abschließenden Abschnitt (III.) soll die mehrsprachige Publikationspraxis hinterfragt und die Bedeutung der Sprachwahl für Schlegels Denken erläutert werden.
Leben und Werke der Brüder Wilhelm (1767−1835) und Alexander (1769−1859) von Humboldt vollzogen sich in vielfältigen Kultur- und Wissenstransfers. Beide waren, in jeweils unterschiedlichem Ausmaß, Forschungsreisende, wissenschaftliche Publizisten, Wissenschaftspolitiker, Staats- und Hofbedienstete. In der Vielfalt dieser Funktionen waren sie darauf angewiesen, zwischen fachlicher, politischer und öffentlicher Kommunkation vermitteln zu können, sich also selbst zu übersetzen - in einem zunächst einmal weiten Verständnis von Übersetzung, das neben sprachlichen Übertragungen auch die "Notwendigkeit kultureller Übersetzungsprozesse" meint und auf ein "Immer-schon-Übersetztsein" von Kulturen in ihrer Vielheit und Mannigfaltigkeit verweist. Solche kulturellen Transfers erweisen sich aber bei den Humboldts auf spezifische Weise als sprachgebunden. Daher lässt sich der im weiteren Sinne übersetzende Charakter ihres wissenschaftlichen und politischen Wirkens auf die interlingualen Selbstübersetzungen hin engführen, die untrennbar mit der mehrsprachigen Genese ihres jeweiligen Gesamtwerks verbunden sind. [...] Als besonderer Fall von kosmopolitischer Mehrsprachigkeit ist für beide Humboldts die deutsch-französische Beziehungs- und Verflechtungsgeschichte betont worden. Für beide besaß die französische Sprache einen zentralen Stellenwert: als von klein auf gesprochene Zweitsprache und als wissenschaftliche lingua franca der Zeit um 1800. Sie war immer dort mit im Spiel, wo sich Wilhelm und Alexander von Humboldt als Selbstübersetzer betätigten. Dabei ging die Übersetzungsrichtung sowohl aus dem Deutschen ins Französische als auch umgekehrt; übersetzt wurden sowohl komplette eigene Texte als auch Abschnitte aus teils publizierten, teils unpublizierten Arbeiten, die in der jeweils anderen Sprache zum Ausgangsmaterial für neue Schriften werden konnten. Auf diese Weise entstanden zweisprachige Textkorpora verschiedenen Zuschnitts, wie im Folgenden an chronologisch angeordneten Beispielen dargelegt werden soll, und zwar sowohl hinsichtlich der jeweiligen wissenschaftlichen Kontexte als auch im mikrologischen Blick auf die Texte selbst. Zwei der Beispiele stammen von Wilhelm von Humboldt: ein deutsch-französisches Konglomerat zur Ästhetik (II.) und ein französisch-deutsches über altamerikanische Sprachen (IV.); die beiden anderen von Alexander von Humboldt: die parallel auf Französisch und Deutsch veröffentlichte Abhandlung zur Geographie der Pflanzen (III.) und die französische Übersetzung der zuerst auf Deutsch publizierten Einleitung zum mehrbändigen Spätwerk, dem Kosmos (V.). Abschließend soll nochmals die pragmatische und theoretische Reichweite der Humboldt'schen Selbstübersetzungen benannt werden (VI.).
Von Alessandro Manzonis 'italienischem' Beitrag zur europäischen Romantik-Debatte, der "Lettre à M.r C*** sur l'unité de temps et de lieu dans la tragédie", gibt es keine italienische Ausgangsversion. Im strengen Sinn handelt es sich bei dem hier infrage stehenden Text also nicht um eine Selbstübersetzung, sondern um ein Schreiben in der Fremdsprache Französisch, für das sich sein Autor gegenstands- und situationsbezogen entscheidet. Gleichzeitig ist bekannt, dass Manzonis Schreiben von französischer Politik, französischer Wissenschaft und Kultur gar nicht zu trennen ist. [...] Manzoni erfindet mit den "Promessi Sposi" Sprache als Dichtung und Dichtung als Sprache, als sogenannte National- und Weltliteratur. Die "Lettre à M. Chauvet" markiert dabei, so möchte ich im Folgenden zeigen, eine Art sprachlichen Wendepunkt, an dem die Sprache zu einem metaphorischen Exil wird und als ebenso kontingent wie notwendig erscheint. Der durch die "Lettre à M. Chauvet" initiierte Wissenstransfer wird bedingt durch die spezifische sprachliche und politische Situation Italiens in der ersten Hälfte des 19. Jahrhunderts. Nur vor diesem Hintergrund wird Manzonis biographische, kulturelle und sprachliche Zwischenposition verständlich. Denn erst im Abgleich der mehrsprachigen Situation (Dialekt, Französisch, hochitalienische Schriftsprache) mit dem Medium einer kodifizierten Schriftsprache (dem Französischen) wird jene Mehrsprachigkeit zu einem Mangel (I.). Die Kluft zwischen geschriebener und gesprochener Sprache wird in der französischen Fremdsprache zu einem epistemischen Zwischenraum, der - je nach Sprecher- und Adressatenperspektive - verschiedene Wissensbereiche betrifft. Editionsphilologisch wird der einzige von Manzoni auf Französisch publizierte Text zu einem Problem von Autorschaft: Co-Autorschaft scheint noch heute (oder gerade heute) philologisch einen Stein des Anstoßes darzustellen (II.). Auf der Ebene des poetologischen Gegenstands zeigt ein Vergleich der frühen Textfassung ('Primo Sbozzo') mit der Druckfassung, dass dieser Text sich im Verlauf der Abfassung mehr und mehr von seinem Ausgangstext (Manzonis Tragödie "Il Conte di Carmagnola" und deren Rezension durch Victor Chauvet) löst und zu einer zukünftigen Poetik der "Promessi Sposi" tendiert (III.). Die kulturelle Zwischenposition des Textes führt dazu, dass der Herausgeber Fauriel auf französischer Seite Manzonis Position als Kritik eines 'Outsiders' gezielt nutzen kann - davon zeugen die textuelle Rahmung wie auch die Missverständnisse, die im Briefwechsel geklärt werden; der Dichter Manzoni wiederum wird in der Perfektionierung des Französischen immer mehr auf das Problem einer sprachlichen Unverständlichkeit des Schriftitalienischen gestoßen (IV.). In der Zusammenfassung lässt sich die "Lettre à M. Chauvet" als offener Text beschreiben, an dem sich, je nach Produktions- und Rezeptionsperspektive, poetologische, subjekttheoretische, kultur- und sprachkritische Fragestellungen kreuzen (V.).
The widely varying therapeutic response of patients with inflammatory bowel disease (IBD) continues to raise questions regarding the unclarified heterogeneity of pathological mechanisms promoting disease progression. While biomarkers for the differentiation of Crohn’s disease (CD) versus ulcerative colitis (UC) have been suggested, specific markers for a CD subclassification in ileal CD versus colonic CD are still rare. Since an altered signature of the tryptophan metabolism is associated with chronic inflammatory disease, we sought to characterize potential biomarkers by focusing on the downstream enzymes and metabolites of kynurenine metabolism. Using immunohistochemical stainings, we analyzed and compared the mucosal tryptophan immune metabolism in bioptic samples from patients with active inflammation due to UC or CD versus healthy controls. Localization-specific quantification of immune cell infiltration, tryptophan-metabolizing enzyme expression and mucosal tryptophan downstream metabolite levels was performed. We found generally increased immune cell infiltrates in the tissue of all patients with IBD. However, in patients with CD, significant differences were found between regulatory T cell and neutrophil granulocyte infiltration in the ileum compared with the colon. Furthermore, we observed decreased kynurenine levels as well as strong kynureninase (KYNU) expression specifically in patients with ileal CD. Correspondingly, significantly elevated levels of the kynurenine metabolite 3-hydroxyanthranilic acid were detected in the ileal CD samples. Highlighting the heterogeneity of the different phenotypes of CD, we identified KYNU as a potential mucosal biomarker allowing the localization-specific differentiation of ileal CD versus colonic CD.
Sphingosine‐1‐phosphate lyase 1 (S1P lyase or SGPL1) is an essential sphingosine‐1‐phosphate‐degrading enzyme. Its manipulation favors onset and progression of colorectal cancer and others in vivo. Thus, SGPL1 is an important modulator of cancer initiation. However, in established cancer, the impact of retrospective SGPL1 modulation is elusive. Herein, we analyzed how SGPL1 siRNA affects malignancy of the human colorectal cancer cells DLD‐1 and found that in parallel to the reduction of SGPL1 expression levels, migration, invasion, and differentiation status changed. Diminished SGPL1 expression was accompanied with reduced cell migration and cell invasion in scratch assays and transwell assays, whereas metabolic activity and proliferation was not altered. Decreased migration was attended by increased cell–cell‐adhesion through upregulation of E‐cadherin and formation of cadherin‐actin complexes. Spreading cell islets showed lower vimentin abundance in border cells. Furthermore, SGPL1 siRNA treatment induced expression of epithelial cell differentiation markers, such as intestinal alkaline phosphatase and cytokeratin 20. Hence, interference with SGPL1 expression augmented a partial redifferentiation of colorectal cancer cells toward normal colon epithelial cells. Our investigation showed that SGPL1 siRNA influenced tumorigenic activity of established colorectal cancer cells. We therefore suggest SGPL1 as a target for lowering malignant potential of already existing cancer.
Measurement of inclusive J/ψ polarization in p + p collisions at √s=200 GeV by the STAR experiment
(2020)
We report on new measurements of inclusive 𝐽/𝜓 polarization at midrapidity in 𝑝+𝑝 collisions at √𝑠=200 GeV by the STAR experiment at the Relativistic Heavy Ion Collider. The polarization parameters, 𝜆𝜃, 𝜆𝜙, and 𝜆𝜃𝜙, are measured as a function of transverse momentum (𝑝T) in both the helicity and Collins-Soper (CS) reference frames within 𝑝T<10 GeV/𝑐. Except for 𝜆𝜃 in the CS frame at the highest measured 𝑝T, all three polarization parameters are consistent with 0 in both reference frames without any strong 𝑝T dependence. Several model calculations are compared with data, and the one using the Color Glass Condensate effective field theory coupled with nonrelativistic QCD gives the best overall description of the experimental results, even though other models cannot be ruled out due to experimental uncertainties.
Cells maintain membrane fluidity by regulating lipid saturation, but the molecular mechanisms of this homeoviscous adaptation remain poorly understood. We have reconstituted the core machinery for regulating lipid saturation in baker’s yeast to study its molecular mechanism. By combining molecular dynamics simulations with experiments, we uncover a remarkable sensitivity of the transcriptional regulator Mga2 to the abundance, position, and configuration of double bonds in lipid acyl chains, and provide insights into the molecular rules of membrane adaptation. Our data challenge the prevailing hypothesis that membrane fluidity serves as the measured variable for regulating lipid saturation. Rather, we show that Mga2 senses the molecular lipid-packing density in a defined region of the membrane. Our findings suggest that membrane property sensors have evolved remarkable sensitivities to highly specific aspects of membrane structure and dynamics, thus paving the way toward the development of genetically encoded reporters for such properties in the future.
Enhanced LTP of population spikes in the dentate gyrus of mice haploinsufficient for neurobeachin
(2020)
Deletion of the autism candidate molecule neurobeachin (Nbea), a large PH-BEACH-domain containing neuronal protein, has been shown to affect synaptic function by interfering with neurotransmitter receptor targeting and dendritic spine formation. Previous analysis of mice lacking one allele of the Nbea gene identified impaired spatial learning and memory in addition to altered autism-related behaviours. However, no functional data from living heterozygous Nbea mice (Nbea+/−) are available to corroborate the behavioural phenotype. Here, we explored the consequences of Nbea haploinsufficiency on excitation/inhibition balance and synaptic plasticity in the intact hippocampal dentate gyrus of Nbea+/− animals in vivo by electrophysiological recordings. Based on field potential recordings, we show that Nbea+/− mice display enhanced LTP of the granule cell population spike, but no differences in basal synaptic transmission, synapse numbers, short-term plasticity, or network inhibition. These data indicate that Nbea haploinsufficiency causes remarkably specific alterations to granule cell excitability in vivo, which may contribute to the behavioural abnormalities in Nbea+/− mice and to related symptoms in patients.
Understanding the nano-architecture of protein machines in diverse subcellular compartments remains a challenge despite rapid progress in super-resolution microscopy. While single-molecule localization microscopy techniques allow the visualization and identification of cellular structures with near-molecular resolution, multiplex-labeling of tens of target proteins within the same sample has not yet been achieved routinely. However, single sample multiplexing is essential to detect patterns that threaten to get lost in multi-sample averaging. Here, we report maS3TORM (multiplexed automated serial staining stochastic optical reconstruction microscopy), a microscopy approach capable of fully automated 3D direct STORM (dSTORM) imaging and solution exchange employing a re-staining protocol to achieve highly multiplexed protein localization within individual biological samples. We demonstrate 3D super-resolution images of 15 targets in single cultured cells and 16 targets in individual neuronal tissue samples with <10 nm localization precision, allowing us to define distinct nano-architectural features of protein distribution within the presynaptic nerve terminal.
This paper describes the addition of Luxembourgish to the language versions of MAIN, the adaption process and the use of MAIN in Luxembourg. A short description of Luxembourg’s multilingual society and trilingual school system as well as an overview of selected morphosyntactic and syntactic features of Luxembourgish introduce the Luxembourgish version of MAIN.
NATURAL LANGUAGE (NL) IS A PROMISING ALTERNATIVE INTERFACE TO DATABASE MANAGEMENT SYSTEMS (DBMSs) BECAUSE IT ENABLES NON-TECHNICAL USERS TO FORMULATE COMPLEX QUESTIONS. RECENTLY, DEEP LEARNING HAS GAINED TRACTION FOR TRANSLATING NATURAL LANGUAGE TO SQL. HOWEVER, THE CORE PROBLEM WITH EXISTING DEEP LEARNING APPROACHES IS THAT THEY REQUIRE AN ENORMOUS AMOUNT OF MANUALLY CURATED TRAINING DATA IN ORDER TO PROVIDE ACCURATE TRANSLATIONS. WE PRESENT DBPAL THAT USES A NOVEL TRAINING PIPELINE TO LEARN NL2SQL INTERFACES WHICH SYNTHESIZES TRAINING DATA AND, THUS, DOES NOT RELY ON MANUALLY CURATED TRAINING DATA.
Background and Objectives: Red blood cell (RBC) transfusions are needed by almost every acute myeloid leukaemia (AML) patient undergoing induction chemotherapy and constitute a cornerstone in supportive measures for cancer patients in general. Randomized controlled trials have shown non‐inferiority or even superiority of restrictive transfusion guidelines over liberal transfusion guidelines in specific clinical situations outside of medical oncology. In this study, we analysed whether more restrictive RBC transfusion reduces blood use without affecting hard outcomes.
Materials and Methods: A total of 352 AML patients diagnosed between 2007 and 2018 and undergoing intensive induction chemotherapy were included in this retrospective analysis. In the less restrictive transfusion group, patients received RBC transfusion for haemoglobin levels below 8 g/dl (2007–2014). In the restrictive transfusion group, patients received RBC transfusion for haemoglobin levels below 7 g/dl (2016–2018). Liberal transfusion triggers were never endorsed.
Results: A total of 268 (76·1%) and 84 (23·9%) AML patients fell into the less restrictive and restrictive transfusion groups, respectively. The less restrictive transfusion group had 1 g/dl higher mean haemoglobin levels, received their first RBC transfusions earlier and needed 1·5 more units of RBC during the hospital stay of induction chemotherapy. Febrile episodes, C‐reactive protein levels, admission to the intensive care unit, length of hospital stay as well as response and survival rates did not differ between the two cohorts.
Conclusion: From our retrospective analysis, we conclude that a more restrictive transfusion trigger does not affect important outcomes of AML patients. The opportunity to test possible effects of the more severe anaemia in the restrictive transfusion group on quality of life was missed.
Vor allem in Deutschland ist die historische Perspektive spätestens seit Dilthey erste (akademische) Bürgerpflicht und Inbegriff von Geisteswissenschaftlichkeit überhaupt. Erfrischend und gründlicher provozierend ist deshalb der Blick in das Buch eines jungen Anglisten der Yale University, das auch in den USA, wo die Humanities von jeher nicht so eng an den Primat der Geschichte gekoppelt waren, für einige Aufregung gesorgt hat. Im Alleingang, abseits geläufiger Periodisierungen und Selbstbeschreibungen, hat Joseph North eine - eingestandenermaßen tendenziöse - Geschichte seines Fachs vorgelegt
Early experiences of childhood sexual or physical abuse are often associated with functional impairments, reduced well-being and interpersonal problems in adulthood. Prior studies have addressed whether the traumatic experience itself or adult psychopathology is linked to these limitations. To approach this question, individuals with posttraumatic stress disorder (PTSD) and healthy individuals with and without a history of child abuse were investigated. We used global positioning system (GPS) tracking to study temporal and spatial limitations in the participants’ real-life activity space over the course of one week. The sample consisted of 228 female participants: 150 women with PTSD and emotional instability with a history of child abuse, 35 mentally healthy women with a history of child abuse (healthy trauma controls, HTC) and 43 mentally healthy women without any traumatic experiences in their past (healthy controls, HC). Both traumatized groups—i.e. the PTSD and the HTC group—had smaller movement radii than the HC group on the weekends, but neither spent significantly less time away from home than HC. Some differences between PTSD and HC in movement radius seem to be related to correlates of PTSD psychopathology, like depression and physical health. Yet group differences between HTC and HC in movement radius remained even when contextual and individual health variables were included in the model, indicating specific effects of traumatic experiences on activity space. Experiences of child abuse could limit activity space later in life, regardless of whether PTSD develops.
In heavy-ion collisions, the quark-gluon plasma is produced far from equilibrium. This regime is currently inaccessible by direct quantum chromodynamics (QCD) computations. In a holographic context, we propose a general method to characterize transport properties based on well-defined two-point functions. We calculate shear transport and entropy far from equilibrium, defining a time-dependent ratio of shear viscosity to entropy density, . Large deviations from its near-equilibrium value , up to a factor of 2.5, are found for realistic situations at the Large Hadron Collider. We predict the far-from-equilibrium time-dependence of to substantially affect the evolution of the QCD plasma and to impact the extraction of QCD properties from flow coefficients in heavy-ion collision data.
Vorwort
(2020)
Lange waren Formkonzepte dem Zug der Zeit entzogen, um dann am Ende des 18. Jahrhunderts, und prominent in Goethes Naturforschung, massiv unter ihren Einfluss zu geraten. Wenn Goethes Überlegungen zu Morphologie und Metamorphose Manifestationen der im späten 18. Jahrhundert auf breiter Front beobachtbaren Verzeitlichungsprozesse darstellen, drängt sich die Frage auf, wie das Verhältnis von Zeit und Form in der als Zeitkunst verstandenen Literatur des Autors wirksam wurde.
Understanding the conformational sampling of translation-arrested ribosome nascent chain complexes is key to understand co-translational folding. Up to now, coupling of cysteine oxidation, disulfide bond formation and structure formation in nascent chains has remained elusive. Here, we investigate the eye-lens protein γB-crystallin in the ribosomal exit tunnel. Using mass spectrometry, theoretical simulations, dynamic nuclear polarization-enhanced solid-state nuclear magnetic resonance and cryo-electron microscopy, we show that thiol groups of cysteine residues undergo S-glutathionylation and S-nitrosylation and form non-native disulfide bonds. Thus, covalent modification chemistry occurs already prior to nascent chain release as the ribosome exit tunnel provides sufficient space even for disulfide bond formation which can guide protein folding.
Einer bekannten Redensart zufolge soll man die Feste feiern, wie sie fallen. Zynisch könnte man fragen: Gilt das auch für Epochenwenden? Sind die auch hinzunehmen wiewiederkehrende Feiertage, Grippewellen oder unerwartete Naturkatastrophen? Dass die Covid-19-Pandemie schon jetzt in ganz unterschiedlichen Zusammenhängen als Epochenwende verstanden wird, merkt man nicht nur an der Häufung des vordem eher vermiedenen Epochenbegriffs, sondern auch am Gebrauch der Formel 'vor und nach Corona' - obwohl doch ein Ende der Pandemie derzeit nicht in Sicht ist und deshalb auch und gerade Feste nicht wie üblich begangen werden können (oder sollten).
Our primary objective is to construct a plausible, unified model of inflation, dark energy and dark matter from a fundamental Lagrangian action first principle, wherein all fundamental ingredients are systematically dynamically generated starting from a very simple model of modified gravity interacting with a single scalar field employing the formalism of non-Riemannian spacetime volume-elements. The non-Riemannian volume element in the initial scalar field action leads to a hidden, nonlinear Noether symmetry which produces an energy-momentum tensor identified as the sum of a dynamically generated cosmological constant and dust-like dark matter. The non-Riemannian volume-element in the initial Einstein–Hilbert action upon passage to the physical Einstein-frame creates, dynamically, a second scalar field with a non-trivial inflationary potential and with an additional interaction with the dynamically generated dark matter. The resulting Einstein-frame action describes a fully dynamically generated inflationary model coupled to dark matter. Numerical results for observables such as the scalar power spectral index and the tensor-to-scalar ratio conform to the latest 2018 PLANCK data.
The Culex pipiens complex encompasses five species and subspecies of the genus Culex. Over time, a multitude of morphologically indistinguishable species has been assigned to this complex with several species being classified as important vectors for different diseases. Some species of this complex hibernate in subterranean habitats, and it has been proven that viruses can survive this phase of hibernation. However, studies focusing on the environmental requirements, ecology and spatial and temporal distribution patterns of mosquitos in underground habitats are sparse. Here, we investigate the main environmental factors and dependencies of Culex, considering the number of individuals and survival probabilities in underground habitats during the winter months. Methods. Since the State of Hesse, Germany harbors about 3500 to 4000 subterranean shelters ample availability of subterranean habitats there provides a good opportunity to conduct detailed investigations of the Culex pipiens complex. In this study, we identified a sample of 727 specimens of overwintering females within the Culex pipiens complex from 52 different underground sites collected over a period of 23 years using qPCR. A complete data set of samplings of hibernating mosquitos from 698 subterranean habitats in Central Germany over the same period was available to study the spatial and temporal patterns and the effect of temperature and precipitation conditions on these hibernating populations using a generalized linear model (GLM). Results. Our qPCR-results show, similar to aboveground studies of mosquitos, that Culex pipiens pipiens and Culex torrentium occur sympatrically. On the other hand, Culex pipiens molestus occurred very rarely. The GLM revealed no shifts in species composition over time, but different preferences for subterranean hibernacula, chemical effects on overwintering populations as well as effects of annual and seasonal mean temperature and precipitation during the active phase from March to November. Cx. p. pipiens and Cx. torrentium are the most common species within Hessian caves and other underground habitats during winter. They co-occur with different frequency without any patterns in species composition. Weather conditions influence the number of overwintering mosquitos during the activity phase. Depending on cave parameters, the number of mosquitos decreases during the winter months.
Maintaining biodiversity and ecosystem function is critical on national and global scales. However, while only a fraction of the global biodiversity is known, its current decline is unprecedented, making biodiversity hotspots a conservation priority. The Sierra Gorda Biodiversity Reserve (SGBR) in Central Mexico is known for its rich biodiversity. It is an example of the juxtaposition between species discovery and extinction: aquatic species richness is mostly unknown as no efforts have investigated aquatic communities so far, but are already anthropogenically stressed. We hypothesized that invasive species are already well established in various protected areas and investigated this by assessing the threat of invasive species that are already established within the SGBR on the native biodiversity. By combining field sampling with peer-reviewed literature and local reports, we identify the presence of various non-native species in SGBR. Among these non-native species identified were opportunistic predatory fish and potentially-pathogen transmitting molluscs, but also, a habitat engineer capable of modifying ecosystem functions. Moreover, we highlight that these species were introduced despite legislation and without any knowledge among authorities. As a result, we underline the necessity to describe native species, control invasive and prevent the introduction of further non-native species. If accelerated action is not taken, we risk losing a considerable amount of described and unknown freshwater biota. Keywords: Anthropocene, Biodiversity loss, Freshwater, Invasive species, Mexico, Nature reserve.
In Eurotransplant kidney allocation system (ETKAS), candidates can be considered unlimitedly for repeated re‐transplantation. Data on outcome and benefit are indeterminate. We performed a retrospective 15‐year patient and graft outcome data analysis from 1464 recipients of a third or fourth or higher sequential deceased donor renal transplantation (DDRT) from 42 transplant centers. Repeated re‐DDRT recipients were younger (mean 43.0 vs. 50.2 years) compared to first DDRT recipients. They received grafts with more favorable HLA matches (89.0% vs. 84.5%) but thereby no statistically significant improvement of patient and graft outcome was found as comparatively demonstrated in 1st DDRT. In the multivariate modeling accounting for confounding factors, mortality and graft loss after 3rd and ≥4th DDRT (P < 0.001 each) and death with functioning graft (DwFG) after 3rd DDRT (P = 0.001) were higher as compared to 1st DDRT. The incidence of primary nonfunction (PNF) was also significantly higher in re‐DDRT (12.7%) than in 1st DDRT (7.1%; P < 0.001). Facing organ shortage, increasing waiting time, and considerable mortality on dialysis, we question the current policy of repeated re‐DDRT. The data from this survey propose better HLA matching in first DDRT and second DDRT and careful selection of candidates, especially for ≥4th DDRT.
Chronische pulmonale Infektionen mit Pseudomonas aeruginosa (PA) betreffen die überwiegende Mehrheit der erwachsenen Mukoviszidose (Cystische Fibrose, CF) Patienten.
Diese Infektionen führen gesichert zu einer Abnahme der Lungenfunktion und Zunahme der Mortalität der Patienten. Atemwegsviren stehen im Verdacht pulmonale Exazerbationen bei CF-Patienten auszulösen. Unklar ist jedoch, welchen Einfluss eine chronische Infektion mit PA auf die Anfälligkeit und Reaktion des Atemwegsepithels auf virale Infektionen hat.
Das Ziel dieser Arbeit war es daher, die Interaktionen zwischen PA, humanen Rhinoviren (HRV) und primären bronchialen Epithelzellen zu untersuchen. Hierfür wurden Zellen von jeweils drei Patienten mit CF und mit Lungenemphysem aus Lungenexplantaten isoliert und in einem speziellen Air- Liquid-Interface Zellkulturmodell zu einem mukoziliär differenzierten mehrreihigen Flimmerepithel kultiviert. Chronische Infektionen wurden mit klinischen PA Isolaten für einen Gesamtzeitraum von 16 Tagen durchgeführt. Anschließend wurden die Zellen mit HRV infiziert. Schlüsselzytokine, Interferone und virale RNA wurden mittels Cytometric bead array, ELISA und qPCR bestimmt.
Rein virale Infektionen mit HRV führten zu einem Anstieg von IL-1, -6, -8, TNF- α, IP10 und IFN-b, IFN-l1 sowie ISGs und in ähnlichem Ausmaß konnte dies auch bei Coinfektionen mit einem mukoiden PA-Isolat beobachtet werden. Coinfektionen mit einem nicht-mukoiden PA-Isolat führten im Vergleich zu rein viralen Infektionen zu vermehrter Expression von IL-1β und IL-6 mRNA. Während es unter diesen Bedingungen auch auf Proteinebene zu einem Anstieg der IL-1β Konzentration kam, lag die Konzentration von freiem IL-6 Protein in nahezu allen Proben unter der Nachweisgrenze. Zellkulturmedium aus Coinfektionen mit diesem nicht-mukoiden PA-Isolat führten zudem zu einem Abbau oder einer Bindung von extern zugegebenen rekombinantem IL-6.
IL-8, IP-10, TNF-α Protein und mRNA von IFN-β, -λ1 und ISGs, sowie die Viruslast waren vergleichbar zwischen rein viralen Infektionen und bakteriell- viralen Coinfektionen. Ebenfalls keine Unterschiede wurden zwischen Zellen von Emphysem und CF-Spendern gefunden. Insgesamt zeigen diese Daten, dass eine PA-Infektion die Antwort differenzierter bronchialer Epithelzellen auf eine Virusinfektion verändern kann. Die hierdurch veränderte Immunantwort und möglicherweise eingeschränkten epithelialen Reparaturmechanismen könnten eine Ursache aggravierter viraler Infektionen in P. aeruginosa-infizierten Atemwegen darstellen.
Ein besseres Verständnis der Interaktionen zwischen chronisch-bakteriellen und viralen Atemwegsinfektionen könnte potenziell die Behandlung virus-induzierter Exazerbationen bei PA-infizierten CF-Patienten verbessern.
The auditory midbrain (inferior colliculus, IC) plays an important role in sound processing, acting as hub for acoustic information extraction and for the implementation of fast audio-motor behaviors. IC neurons are topographically organized according to their sound frequency preference: dorsal IC regions encode low frequencies while ventral areas respond best to high frequencies, a type of sensory map defined as tonotopy. Tonotopic maps have been studied extensively using artificial stimuli (pure tones) but our knowledge of how these maps represent information about sequences of natural, spectro-temporally rich sounds is sparse. We studied this question by conducting simultaneous extracellular recordings across IC depths in awake bats (Carollia perspicillata) that listened to sequences of natural communication and echolocation sounds. The hypothesis was that information about these two types of sound streams is represented at different IC depths since they exhibit large differences in spectral composition, i.e., echolocation covers the high-frequency portion of the bat soundscape (> 45 kHz), while communication sounds are broadband and carry most power at low frequencies (20–25 kHz). Our results showed that mutual information between neuronal responses and acoustic stimuli, as well as response redundancy in pairs of neurons recorded simultaneously, increase exponentially with IC depth. The latter occurs regardless of the sound type presented to the bats (echolocation or communication). Taken together, our results indicate the existence of mutual information and redundancy maps at the midbrain level whose response cannot be predicted based on the frequency composition of natural sounds and classic neuronal tuning curves.
Measurement of inclusive charged-particle jet production in Au + Au collisions at √sNN=200 GeV
(2020)
The STAR Collaboration at the Relativistic Heavy Ion Collider reports the first measurement of inclusive jet production in peripheral and central Au+Au collisions at √𝑠𝑁𝑁=200 GeV. Jets are reconstructed with the anti-𝑘𝑇 algorithm using charged tracks with pseudorapidity |𝜂|<1.0 and transverse momentum 0.2<𝑝ch
𝑇,jet<30 GeV/𝑐, with jet resolution parameter 𝑅=0.2, 0.3, and 0.4. The large background yield uncorrelated with the jet signal is observed to be dominated by statistical phase space, consistent with a previous coincidence measurement. This background is suppressed by requiring a high-transverse-momentum (high-𝑝𝑇) leading hadron in accepted jet candidates. The bias imposed by this requirement is assessed, and the 𝑝𝑇 region in which the bias is small is identified. Inclusive charged-particle jet distributions are reported in peripheral and central Au+Au collisions for 5<𝑝ch
𝑇,jet<25 GeV/𝑐 and 5<𝑝ch
𝑇,jet<30 GeV/𝑐, respectively. The charged-particle jet inclusive yield is suppressed for central Au+Au collisions, compared to both the peripheral Au+Au yield from this measurement and to the 𝑝𝑝 yield calculated using the PYTHIA event generator. The magnitude of the suppression is consistent with that of inclusive hadron production at high 𝑝𝑇 and that of semi-inclusive recoil jet yield when expressed in terms of energy loss due to medium-induced energy transport. Comparison of inclusive charged-particle jet yields for different values of 𝑅 exhibits no significant evidence for medium-induced broadening of the transverse jet profile for 𝑅 <0.4 in central Au+Au collisions. The measured distributions are consistent with theoretical model calculations that incorporate jet quenching.
Die Besonderheiten der Gutachtenkultur verdanken sich demselben Umstand: Das geisteswissenschaftliche Gutachten ist in all seinen Varianten, vom Referenzschreiben für eine Person (im Englischen 'letter of recommendation') bis zum anonymen Gutachten eines Verbundprojektes, stets ein Hybrid aus Patronage und Sachverständigen- bzw. Expertenmeinung. Dabei gibt es auf Sender- und Empfängerseite unausgesprochene Erwartungshaltungen, Usancen und Codes, die die Vergleichbarkeit von Gutachten so sichern sollen, dass sie eine Entscheidungshilfe darstellen.
Hölderlin und Hegel heute
(2020)
Die Wege des Dichters und des Philosophen, die sich in revolutionären Zeiten im Tübinger Stift kennengelernt hatten, waren verschieden und doch vielfältig verbunden. Immer wieder und besonders häufig in diesem doppelten Jubiläumsjahr 2020 sind die Dioskuren des deutschen Idealismus Gegenstand der Betrachtung und Bewunderung gewesen. [...] Am 9. Dezember 2020 wollen wir uns unter dem Titel "Hölderlin und Hegel heute" den Werken dieser beiden Schwaben jedoch vor allem unter der Fragestellung nähern, was diese denn mit uns heute noch oder wieder zu tun haben könnten.
Marie Holzman, 1922–1941
(2020)
Marie Holzman, geboren am 22. April 1922 in Jena, war die ältere Tochter des seit 1922/23 in Kaunas (Litauen) ansässigen Gründers und Inhabers der Verlagsbuchhandlung Pribačis Max Holzman (1889–1941) sowie der aus Jena stammenden Malerin und Kunsterzieherin Helene Czapski-Holzman (1891–1961). Nach dem deutschen Überfall auf die Sowjetunion wurde sie am 29. Oktober 1941 in Kaunas ermordet. Ihre Mutter hat zwei von ihrer Tochter aus dem Litauischen übersetzte Erzählungen bewahrt. Unlängst gelangten die beiden Manuskripte ans Exilarchiv der DNB in Frankfurt/M.
First, we propose a scale-invariant modified gravity interacting with a neutral scalar inflaton and a Higgs-like SU(2)×U(1) iso-doublet scalar field based on the formalism of non-Riemannian (metric-independent) spacetime volume-elements. This model describes, in the physical Einstein frame, a quintessential inflationary scenario driven by the “inflaton” together with the gravity-“inflaton” assisted dynamical spontaneous SU(2)×U(1) symmetry breaking in the post-inflationary universe, whereas the SU(2)×U(1) symmetry remains intact in the inflationary epoch. Next, we find the explicit representation of the latter quintessential inflationary model with a dynamical Higgs effect as an Eddington-type purely affine gravity.
Background: More than 170 species of tabanids are known in Europe, with many occurring only in limited areas or having become very rare in the last decades. They continue to spread various diseases in animals and are responsible for livestock losses in developing countries. The current monitoring and recording of horseflies is mainly conducted throughout central Europe, with varying degrees of frequency depending on the country. To the detriment of tabanid research, little cooperation exists between western European and Eurasian countries.
Methods: For these reasons, we have compiled available sources in order to generate as complete a dataset as possible of six horsefly species common in Europe. We chose Haematopota pluvialis, Chrysops relictus, C. caecutiens, Tabanus bromius, T. bovinus and T. sudeticus as ubiquitous and abundant species within Europe. The aim of this study is to estimate the distribution, land cover usage and niches of these species. We used a surface-range envelope (SRE) model in accordance with our hypothesis of an underestimated distribution based on Eurocentric monitoring regimes.
Results: Our results show that all six species have a wide range in Eurasia, have a broad climatic niche and can therefore be considered as widespread generalists. Areas with modelled habitat suitability cover the observed distribution and go far beyond these. This supports our assumption that the current state of tabanid monitoring and the recorded distribution significantly underestimates the actual distribution. Our results show that the species can withstand extreme weather and climatic conditions and can be found in areas with only a few frost-free months per year. Additionally, our results reveal that species prefer certain land-cover environments and avoid other land-cover types.
Conclusions: The SRE model is an effective tool to calculate the distribution of species that are well monitored in some areas but poorly in others. Our results support the hypothesis that the available distribution data underestimate the actual distribution of the surveyed species.
Healthy and degenerating intervertebral discs (IVDs) are innervated by sympathetic nerves, however, adrenoceptor (AR) expression and functionality have never been investigated systematically. Therefore, AR gene expression was analyzed in both tissue and isolated cells from degenerated human IVDs. Furthermore, human IVD samples and spine sections of wildtype mice (WT) and of a mouse line that develops spontaneous IVD degeneration (IVDD, in SM/J mice) were stained for ARs and extracellular matrix (ECM) components. In IVD homogenates and cells α1a-, α1b-, α2a-, α2b-, α2c-, β1-, and β2-AR genes were expressed. In human sections, β2-AR was detectable, and its localization parallels with ECM alterations. Similarly, in IVDs of WT mice, only β2-AR was expressed, and in IVDs of SM/J mice, β2AR expression was stronger accompanied by increased collagen II, collagen XII, decorin as well as decreased cartilage oligomeric matrix protein expression. In addition, norepinephrine stimulation of isolated human IVD cells induced intracellular signaling via ERK1/2 and PKA. For the first time, the existence and functionality of ARs were demonstrated in IVD tissue samples, suggesting that the sympathicus might play a role in IVDD. Further studies will address relevant cellular mechanisms and thereby help to develop novel therapeutic options for IVDD.
Historic amphibian settlements in the northwestern Nile delta - a geoarchaeological perspective
(2020)
No concise picture of the archaeological and palaeoecological evolution can be drawn for the northwestern Nile delta, and archaeological records show significant population dynamics that still need explanation and spur the need for further palaeoenvironmental research. This study delivers a set of new methods especially in the fields of remote sensing and data analytics that can be regarded as important milestones and foundations for further palaeoenvironmental research in the area. Additionally, it shows new insights for individual time slices.
This geoarchaeological project is a cooperation with the archaeological excavations of the German Archaeological Institute (DAI) in Buto and Kom el’Gir. It expands the work of Wunderlich (1989) which laid important foundations in understanding the origin of the initial landscape that was later colonized in different cultural stages showing different dynamics, settlement intensities and even long phases of abandonment or breaks in between. This forms the starting point for relating the population dynamics of the different cultural phases reaching from Predynastic (prior to 3150 before Christ) up to the Greco-Roman era (~anno Domini 650) to the environmental history and events that occurred in the area. It is very likely that environmental changes such as the shifting of major water routes, inundation or paludification of larger areas or other environmental events affected settlements and human life in the area.
In the fields of remote sensing new methods are presented to complete information on the location of ancient settlements, and complex workflows are developed that allow the tracing of subsurface structures via indirect analysis of vegetation growth in larger time series data. It was verified that a relationship exists between vegetation performance, the appearance of archaeologic material in the topsoil, and the location of former Nile river branches.
Together with a new high resolution digital elevation model (DEM) based on TanDEM-X data, new interpretations with a high spatial significance are possible. For individual time slices, namely the Late Dynastic and Greco-Roman era, this work delivers a detailed landscape description suggesting a finely ramified subdelta, with all settlements placed on alluvial levees. This explains the massive increase in settlements in the Ptolemaic, Roman and in particular late Roman periods (4th century before Christ – anno Domini 7th century).
We sampled the Nile delta clays together with the channels and the material of the archaeologic excavations in vibracores and profile walls. This geologic inspection of the subsurface together with geochemical results from a handheld portable X-ray fluorescence device (pXRF) allowed new interpretations of the landscape and environmental history. For example, we used geochemical data to distinguish between artificial and natural channels as a measure for the anthropogenic influence, a proxy for past environmental characteristics and lastly as a basis for a new dating method. Many of the channels, for instance, were dated by our own 14C datings, comparisons with the previous work ofWunderlich (1989) and application of new dating approach based on machine learning with artificial neural networks. Additionally, we run a full methodological approach, and examine the applicability of pXRF methods in general, and test the quality of the data to detect distinct geochemical differences between the main settlement phases with advanced methods in data analytics. The dating is based, for example, on the training of artificial neural networks with pXRF data from archaeological material of well-dated context to date test data of cultural layers within the vibracores. With this method the homogeneous Nile alluvium, cultural layers and channels can be dated roughly and, as a result, fundamental changes in the landscape can be linked with the settlement history of Buto and neighboring tells.
Inappropriate land management leads to soil loss with destruction of the land’s resource and sediment input into the receiving river. Part of the sediment budget of a catchment is the estimation of soil loss. In the Ruzizi catchment in the Eastern Democratic Republic of the Congo (DRC), only limited research has been conducted on soil loss mainly dealing with local observations on geomorphological forms or river load measurements; a regional quantification of soil loss is missing so far. Such quantifications can be calculated using the Universal Soil Loss Equation (USLE). It is composed of four factors: precipitation (R), soil (K), topography (LS), and vegetation cover (C). The factors can be calculated in different ways according to the characteristics of the study area. In this paper, different approaches for calculating the single factors are reviewed and validated with field work in two sub-catchments of Ruzizi River supplying the water for the reservoirs of Ruzizi I and II hydroelectric dams. It became obvious that the (R)USLE model provides the best results with revised R and LS factors. C factor calculations required to conduct a supervised classification using the Maximum Likelihood Procedure. Different C factor values were assigned to the land cover classes. The calculations resulted in a soil loss rate for the predominantly occurring Ferralsols and Leptosols of around 576 kt/yr in both catchments, when 2016 landcover and precipitation are used. This represents an area-normalized value of 40.4 t/ha/yr for Ruzizi I and 50.5 t/ha/yr for Ruzizi II due to different landcover in the two sub-catchments. The mean value for the whole study area is 47.8 t/ha/yr or even 27.1 t/ha/yr when considering land management techniques like terracing on the slopes (P factor). This work has shown that the (R)USLE model can serve as an easy to handle tool for soil loss quantification when comprehensive field work results are sparse. The model can be implemented in Geographic Information Systems (GIS) with free data; hence, a validation is crucial. It becomes apparent that the use of high resolution Sentinel 2a MSI data as the basis for C factor calculations is an appropriate method for considering heterogeneous Land Use Land Cover (LULC) patterns. To transfer the approach to other regions, the calculation of factor R needs to be modified
During the 2016-17 and 2018-19 running periods, the BESIII experiment collected 7.5~fb−1 of e+e− collision data at center-of-mass energies ranging from 4.13 to 4.44~GeV. These data samples are primarily used for the study of excited charmonium and charmoniumlike states. By analyzing the di-muon process e+e−→(γISR/FSR)μ+μ−, we measure the center-of-mass energies of the data samples with a precision of 0.6 MeV. Through a run-by-run study, we find that the center-of-mass energies were stable throughout most of the data-taking period.
There has recently been a dramatic renewal of interest in hadron spectroscopy and charm physics. This renaissance has been driven in part by the discovery of a plethora of charmonium-like XYZ states at BESIII and B factories, and the observation of an intriguing proton-antiproton threshold enhancement and the possibly related X(1835) meson state at BESIII, as well as the threshold measurements of charm mesons and charm baryons.
We present a detailed survey of the important topics in tau-charm physics and hadron physics that can be further explored at BESIII during the remaining operation period of BEPCII. This survey will help in the optimization of the data-taking plan over the coming years, and provides physics motivation for the possible upgrade of BEPCII to higher luminosity.
Using 2.93 fb−1 of 𝑒+𝑒− annihilation data collected at a center-of-mass energy √𝑠=3.773 GeV with the BESIII detector operating at the BEPCII collider, we search for the semileptonic 𝐷0(+) decays into a 𝑏1(1235)−(0) axial-vector meson for the first time. No significant signal is observed for either charge combination. The upper limits on the product branching fractions are ℬ𝐷0→𝑏1(1235)−𝑒+𝜈𝑒·ℬ𝑏1(1235) −→ 𝜔𝜋−<1.12×10−4 and ℬ𝐷+→𝑏1(1235)0𝑒+𝜈𝑒·ℬ𝑏1(1235)0→𝜔𝜋0<1.75×10−4 at the 90% confidence level.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape, followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
Guanosine triphosphate (GTP) cyclohydrolase I (GCH1) catalyzes the conversion of GTP to dihydroneopterin triphosphate (H2NTP), the initiating step in the biosynthesis of tetrahydrobiopterin (BH4). Besides other roles, BH4 functions as cofactor in neurotransmitter biosynthesis. The BH4 biosynthetic pathway and GCH1 have been identified as promising targets to treat pain disorders in patients. The function of mammalian GCH1s is regulated by a metabolic sensing mechanism involving a regulator protein, GCH1 feedback regulatory protein (GFRP). GFRP binds to GCH1 to form inhibited or activated complexes dependent on availability of cofactor ligands, BH4 and phenylalanine, respectively. We determined high-resolution structures of human GCH1−GFRP complexes by cryoelectron microscopy (cryo-EM). Cryo-EM revealed structural flexibility of specific and relevant surface lining loops, which previously was not detected by X-ray crystallography due to crystal packing effects. Further, we studied allosteric regulation of isolated GCH1 by X-ray crystallography. Using the combined structural information, we are able to obtain a comprehensive picture of the mechanism of allosteric regulation. Local rearrangements in the allosteric pocket upon BH4 binding result in drastic changes in the quaternary structure of the enzyme, leading to a more compact, tense form of the inhibited protein, and translocate to the active site, leading to an open, more flexible structure of its surroundings. Inhibition of the enzymatic activity is not a result of hindrance of substrate binding, but rather a consequence of accelerated substrate binding kinetics as shown by saturation transfer difference NMR (STD-NMR) and site-directed mutagenesis. We propose a dissociation rate controlled mechanism of allosteric, noncompetitive inhibition.
Selectivity remains a challenge for ATP-mimetic kinase inhibitors, an issue that may be overcome by targeting unique residues or binding pockets. However, to date only few strategies have been developed. Here we identify that bulky residues located N-terminal to the DFG motif (DFG-1) represent an opportunity for designing highly selective inhibitors with unexpected binding modes. We demonstrate that several diverse inhibitors exerted selective, non-canonical binding modes that exclusively target large hydrophobic DFG-1 residues present in many kinases including PIM, CK1, DAPK and CLK. Using the CLK family as a model, structural and biochemical data revealed that the DFG-1 valine controlled a non-canonical binding mode in CLK1, providing a rational for selectivity over the closely-related CLK3 which harbors a smaller DFG-1 alanine. Our data suggests that targeting the restricted back pocket in the small fraction of kinases that harbor bulky DFG-1 residues offers a versatile selectivity filter for inhibitor design.
We report a study of the processes of e+e−→K+(D−sD∗0+D∗−sD0) based on e+e− annihilation samples collected with the BESIII detector operating at BEPCII at five center-of-mass energies ranging from 4.628 to 4.698 GeV with a total integrated luminosity of 3.7 fb−1. An excess over the known contributions of the conventional charmed mesons is observed near the D−sD∗0 and D∗−sD0 mass thresholds in the K+ recoil-mass spectrum for events collected at s√=4.681 GeV. The structure matches a mass-dependent-width Breit-Wigner line shape, whose pole mass and width are determined as (3982.5+1.8−2.6±2.1) MeV/c2 and (12.8+5.3−4.4±3.0) MeV, respectively. The first uncertainties are statistical and the second are systematic. The significance of the resonance hypothesis is estimated to be 5.3 σ over the pure contributions from the conventional charmed mesons. This is the first candidate of the charged hidden-charm tetraquark with strangeness, decaying into D−sD∗0 and D∗−sD0. However, the genuine properties of the excess need further exploration with more statistics.
In the context of workplace health promotion, physical activity programs have been shown to reduce musculoskeletal diseases and stress, and to improve the quality of life. The aim of this study was to examine the effects of using the “five-Business” stretch training device for office workers on their quality of life. A total of 313 office workers (173m/137f) participated voluntarily in this intervention–control study with an average age of 43.37 ± 11.24 (SD) years, 175.37 ± 9.35 cm in height and 75.76 ± 15.23 kg in weight, with an average BMI of 24.5 ± 3.81 kg/m2. The participants completed the stretch training twice a week for approximately 10 minutes for a duration of 12 weeks. The SF-36 questionnaire was used to evaluate the effectiveness of the intervention at baseline and after 12 weeks. Significantly improved outcomes in mental sum score (p = 0.008), physical functioning (p < 0.001), bodily pain (p = 0.01), vitality (p = 0.025), role limitations due to physical problems (p = 0.018) and mental health (p = 0.012) were shown after the stretching training. The results suggest that a 12-week stretching program for office desk workers is suitable to improve significantly their health-related quality of life.
The occupation of dental assistants (DAs) involves many health risks of the musculoskeletal system due to static and prolonged work, which can lead to musculoskeletal disorders (MSDs). The aim of the study was to investigate the prevalence of MSDs in DAs in Germany. Methods: For this purpose, an online questionnaire analyzed 406 (401 female participants and 5 male participants, 401w/5m) DAs. It was based on the Nordic Questionnaire (lifetime, 12-month, and seven-day MSDs’ prevalence separated into neck, shoulder, elbow, wrist, upper back, lower back, hip, knee, and ankle), and occupational and sociodemographic questions as well as questions about specific medical conditions. Results: 98.5% of the participants reported complaints of at least one body region in their lives, 97.5% reported at least one complaint in the last 12 months and 86.9% affirmed at least one complaint in the last seven days. For lifetime, 12-month and seven-day prevalence, the neck was the region that was most affected followed by the shoulder, the upper back and the lower back. Conclusion: The prevalence of MSDs among German (female) DAs was very high. The most affected area is the neck, followed by the shoulder, the lower back, and the upper back. It, therefore, seems necessary to devote more attention to ergonomics at the working practice of DAs as well in education and in dental work.
Background: Musculoskeletal disorders (MSD) are common among dental professionals. The most common areas affected are the trunk, neck, shoulders and wrists. Current evidence suggests that the causes of MSD can be found in the physical demands of the profession. Posture and movement during treatment is influenced by the arrangement of the treatment concept (patient chair, equipment and cabinets). It has not been investigated whether the ergonomic risk differs between the treatment concepts.
Methods: To evaluate the prevalence of MSD in dental professionals, 1000 responses will be collected from a nationwide (Germany) online questionnaire (mod. Nordic Questionnaire and mod. Meyer questionnaire). In order to assess the ergonomic risk of the treatment techniques used in the four treatment concepts, 3D movement analyses are carried out with inertial sensors. For this purpose, 20 teams of dentists and dental assistants from four dental fields of specializations (generalists, orthodontists, endodontists and oral surgeons) and a student control group will be recruited. Each team will execute field specific standardized treatments at a dummy head. Measurements are carried out in each of the four treatment concepts. The data will be analyzed using the Rapid Upper Limb Assessment (RULA) which will be modified for the evaluation of objective data.
Conclusions: On the basis of these investigations, a substantial gain of knowledge regarding work-related MSD in the field of dentistry and its potential biomechanical causes is possible. For the first time, objective and differentiated comparisons between the four treatment concepts are possible for different fields of dental specialization. Up to now, statically held positions of the trunk and proximal upper extremities, but also the repetitive movements of the hands have been considered a risk for MSD. Since both are included in the RULA, dental activities can be assessed in a detailed but also global manner with regard to ergonomic risks.
Zur ergonomischen Beurteilung von Arbeitsplätzen werden „ergonomic risk assessment tools“ (ERAT) verwendet. Mithilfe dieser kann die körperliche Belastung evaluiert und hinsichtlich eines biomechanischen Überlastungsrisikos bewertet werden. Dazu gehören neben Eigenangaben auch observatorische Methoden, deren Ergebnisse in Punktwerten („Scores“) zusammengefasst werden, wie z. B. die RULAMethode („rapid upper limb assessment“). Durch die technische Weiterentwicklung direkter Messmethoden können inertiale Motion-Capture-Systeme im 21. Jahrhundert präzise und kontinuierliche objektive Daten liefern. In einem neuen Ansatz wurde die observatorische Scoring-Methode RULA modifiziert und auf die digital erhobenen Daten angewendet, was differenzierte ergonomische Betrachtungen ganzer Arbeitsabläufe ermöglicht.
The dodecin of Mycobacterium tuberculosis : biological function and biotechnical applications
(2020)
Biological Function of Bacterial Dodecins
In this thesis, the dodecins of Mycobacterium tuberculosis (MtDod), Streptomyces coelicolor (ScDod) and Streptomyces davaonensis (SdDod) were studied. Kinetic measurements of the flavin binding of MtDod revealed that the dodecin binding pocket is filled in two distinct steps, for which a kinetic model then was established and verified by experimental data. The analysis with the two-step model showed that the unique binding pocket of dodecins allows them to bind excessive amounts of flavins, while at low flavin concentrations, flavin is released and only weakly bound. This function of flavin buffering prevents accumulation of free oxidised flavins and therefore helps to keep the redox balance of the cell and prevents potential cell damage caused by excessive free flavins. To further gain insights into the role of bacterial dodecins, the effect of knocking out the dodecin encoding gene in S. davaonensis was analysed. The knockout strain showed increased concentrations of various stress related metabolites, indicating that without dodecin the cellular balance is disrupted, which supports the role of dodecins as a flavin homeostasis factor.
With a self-designed affinity measurement method based on the temperature dependent dissociation of the dodecin:flavin complex, which allowed parallel screening of multiple conditions, it was shown that MtDod, ScDod and SdDod have much higher affinities towards FMN and FAD under acidic conditions. Under these conditions, the three dodecins might function as a FMN storage. M. tuberculosis encounters multiple acidic environments during its infection cycle of humans and can adopt a state of dormancy. During recovery from the dormant state, a flavin storage might be beneficial. For some Streptomyces species it was reported that the formed spores are slightly acidic and therefore ScDod and SdDod could function as flavin storages for the spores. Further details on the flavin binding mechanism of MtDod were revealed by a mutagenesis study, identifying the importance of a histidine residue at the fourth position of the protein sequence for flavin binding, but contrary to expectations, this residue seems only to be partly involved in the pH related affinity shift.
The data, reported in this thesis, demonstrates that bacterial dodecins likely function as flavin homeostasis factors, which allow overall higher flavin pools in the cell without disrupting the cellular balance. Further, the reported acid-dependent increase in binding affinity suggests that under certain conditions bacterial dodecins can also function as a flavin storage system.
Application of the Dodecin of M. tuberculosis
In this thesis, the stability of MtDod, ScDod SdDod and HsDod was analysed to find a suitable dodecin for the use as a carrier/scaffold. Therefore, a method to easily measure the stability of dodecins was designed, which measures the ability of the dodecamer to rebind flavins after a heating phase with stepwise increasing temperatures. Using this assay and testing the stability against detergents by SDS PAGE, showed that the dodecamer of MtDod possesses an excellent stability against a vast array of conditions, like temperatures above 95 °C, low pH and about 2% SDS. By solving the crystal structure of ScDod and SdDod, the latter forming a less stable dodecamer, combined with a mutagenesis study, the importance of a specific salt bridge for dodecamer stability was revealed and might be helpful to find further highly stable dodecins.
In addition to the intrinsic high stability of the MtDod dodecamer, also the robustness of the fold was tested by creating diverse MtDod fusion constructs and producing them in Escherichia coli. Here it was shown that MtDod easily tolerates the attachment of proteins up to 4-times of its own size and that both termini can be modified without affecting the dodecamer noticeably. Further, it was shown that MtDod and many MtDod fusion constructs could be purified in high yields via a protocol based on the removal of E. coli proteins through heat denaturation and subsequent centrifugation. In a case study, by fusing diverse antigens from mostly human proteins to MtDod and using these constructs to produce antibodies in rabbits, it was demonstrated that MtDod is immunogenic and presents the attached antigens to the immune system.
The here reported properties of MtDod and to a lesser degree of other bacterial dodecins, show that bacterial dodecins are a valuable addition to the pool of scaffold and carrier proteins and have great potential as antigen carriers.
This manuscript-based thesis is divided into four chapters. Chapter one is an introduction to lichens and the Antarctic. It introduces the goal of the thesis and the problems related with lichen systematics and the lack of knowledge about Antarctic lichens. The Antarctic is one of the last wildernesses, isolated from the other continents by the Antarctic Circumpolar Current, the Subantarctic Front, the Antarctic Polar Front, and the Drake Passage. Terrestrial life in Antarctica is restricted to widely separated and small ice-free areas that cover only 0.3% of the continent. Colonization of the Antarctic is a challenge for many taxa and is related to their ability for long-range dispersal and their adaptation to the harsh climate. Antarctic terrestrial ecosystems are significantly threatened by climate change, invasive species, and their interactions. Glacial retreat caused by higher than average temperatures exposes new habitats that can be easily colonized from local biota, but non-native species can also be favored by the new climatic conditions. In addition, propagule movement mediated by humans can introduce new species or change the population structure of many taxa. The terrestrial biota is comprised almost exclusively by “lower organisms” (invertebrates, bryophytes, algae, lichenized fungi, and microorganisms). Lichens are the dominant component, and the most important primary producers. Lichens are symbiotic associations consisting of a fungus (mycobiont) and one or more photosynthetic (photobiont) partners. They can disperse sexually or vegetatively. There are several problems related to the symbiotic nature of lichens that do not facilitate easy identification; although molecular data offers additional evidence, species delimitation in lichens is still not straightforward. The true number of species is underestimated due to the presence of cryptic species and species pairs. Recommended universal fungal barcode sequences (e. g. ITS) sometimes fail to delimit species pairs. Thus, it is necessary to identify fast-evolving markers that allow for the delimitation of closely related species before proceeding with the analysis of lichen populations. The goal of this thesis is to elucidate the so far unknown genetic structure among Antarctic lichen populations because of the immediate consequences for conservation strategies. The thesis focuses not only on patterns of differentiation and gene flow, but also investigates the question of human-mediated propagule transfer into Antarctica and among Antarctic sites. This project provides data on the genetic structure of Antarctic lichens that is urgently needed to develop conservation strategies in the face of global warming and increased human activities in the region. Due to the fact that it is not possible to apply all of the unspecific fingerprinting methods to lichens, microsatellites or simple sequence repeats (SSRs) are one of the best tools to investigate the genetic structure of lichen populations. SSRs offer the possibility to discriminate the lichen partners, but species-specific microsatellites have been developed for only a few species. Regarding the Antarctic, only one species has been studied with SSRs.
The second chapter describes new methods and tools to delimit closely related species of lichens and provides fast evolving markers to characterize their genetic structure. The chapter introduces the lichen species analysed in this thesis and the problems related to their correct identification by morphological methods and molecular data. Chapter two explains the sampling methods for lichen populations and the localities from small areas in which the species pairs occur together. Then the methods used to generate and validate fungal specific microsatellites that cross-amplify species pairs are described. This chapter focuses on the species pair Usnea antarctica and U. aurantiacoatra because they are the most common lichens in the Maritime Antarctic. An internal transcribed spacer (ITS) marker do not discriminate between these species, and some authors have suggested to synonymize them. Unpublished results from another Antarctic species pair, Placopsis antarctica and P. contortuplicata, are included to confirm the capability of SSRs to discriminate closely related lichen species. This thesis is the first study to generate SSRs that cross amplify species pairs, using BLAST to compare one genome against the other to obtain markers with the same length in flanking regions. The de novo developed SSRs are able to discriminate the two closely related species, and can detect variability at the population level. In the end of the chapter, ITS sequences, microsatellites, and SNPs are used to delimit the species of Usnea antarctica and U. aurantiacoatra. The chapter exposes the importance of a correct species delimitation and the ability of SSRs and SNPs to delimit the Antarctic Usnea species pair compared with the recommended universal fungal barcode sequence ITS. ...
The β-carboline alkaloid harmine is a potent DYRK1A inhibitor, but suffers from undesired potent inhibition of MAO-A, which strongly limits its application. We synthesized more than 60 analogues of harmine, either by direct modification of the alkaloid or by de novo synthesis of β-carboline and related scaffolds aimed at learning about structure-activity relationships for inhibition of both DYRK1A and MAO-A, with the ultimate goal of separating desired DYRK1A inhibition from undesired MAO-A inhibition. Based on evidence from published crystal structures of harmine bound to each of these enzymes, we performed systematic structure modifications of harmine yielding DYRK1A-selective inhibitors characterized by small polar substituents at N-9 (which preserve DYRK1A inhibition and eliminate MAO-A inhibition) and beneficial residues at C-1 (methyl or chlorine). The top compound AnnH75 remains a potent DYRK1A inhibitor, and it is devoid of MAO-A inhibition. Its binding mode to DYRK1A was elucidated by crystal structure analysis, and docking experiments provided additional insights for this attractive series of DYRK1A and MAO-A inhibitors.
Characterization of a dual BET/HDAC inhibitor for treatment of pancreatic ductal adenocarcinoma
(2020)
Pancreatic ductal adenocarcinoma (PDAC) is resistant to virtually all chemo‐ and targeted therapeutic approaches. Epigenetic regulators represent a novel class of drug targets. Among them, BET and HDAC proteins are central regulators of chromatin structure and transcription, and preclinical evidence suggests effectiveness of combined BET and HDAC inhibition in PDAC. Here, we describe that TW9, a newly generated adduct of the BET inhibitor (+)‐JQ1 and class I HDAC inhibitor CI994, is a potent dual inhibitor simultaneously targeting BET and HDAC proteins. TW9 has a similar affinity to BRD4 bromodomains as (+)‐JQ1 and shares a conserved binding mode, but is significantly more active in inhibiting HDAC1 compared to the parental HDAC inhibitor CI994. TW9 was more potent in inhibiting tumor cell proliferation compared to (+)‐JQ1, CI994 alone or combined treatment of both inhibitors. Sequential administration of gemcitabine and TW9 showed additional synergistic antitumor effects. Microarray analysis revealed that dysregulation of a FOSL1‐directed transcriptional program contributed to the antitumor effects of TW9. Our results demonstrate the potential of a dual chromatin‐targeting strategy in the treatment of PDAC and provide a rationale for further development of multitarget inhibitors.
Extracellular signal-regulated kinase 3 (ERK3), known also as mitogen-activated protein kinase 6 (MAPK6), is an atypical member of MAPK kinase family, which has been poorly studied. Little is known regarding its function in biological processes, yet this atypical kinase has been suggested to play important roles in the migration and invasiveness of certain cancers. The lack of tools, such as a selective inhibitor, hampers the study of ERK3 biology. Here, we report the crystal structure of the kinase domain of this atypical MAPK kinase, providing molecular insights into its distinct ATP binding pocket compared to the classical MAPK ERK2, explaining differences in their inhibitor binding properties. Medium-scale small molecule screening identified a number of inhibitors, several of which unexpectedly exhibited remarkably high inhibitory potencies. The crystal structure of CLK1 in complex with CAF052, one of the most potent inhibitors identified for ERK3, revealed typical type-I binding mode of the inhibitor, which by structural comparison could likely be maintained in ERK3. Together with the presented structural insights, these diverse chemical scaffolds displaying both reversible and irreversible modes of action, will serve as a starting point for the development of selective inhibitors for ERK3, which will be beneficial for elucidating the important functions of this understudied kinase.
Unc-51-like kinase 4 (ULK4) is a pseudokinase that has been linked to the development of several diseases. Even though sequence motifs required for ATP binding in kinases are lacking, ULK4 still tightly binds ATP and the presence of the co-factor is required for structural stability of ULK4. Here, we present a high-resolution structure of a ULK4-ATPγS complex revealing a highly unusual ATP binding mode in which the lack of the canonical VAIK motif lysine is compensated by K39, located N-terminal to αC. Evolutionary analysis suggests that degradation of active site motifs in metazoan ULK4 has co-occurred with an ULK4-specific activation loop, which stabilizes the C helix. In addition, cellular interaction studies using BioID and biochemical validation data revealed high confidence interactors of the pseudokinase and armadillo repeat domains. Many of the identified ULK4 interaction partners were centrosomal and tubulin-associated proteins and several active kinases suggesting interesting regulatory roles for ULK4.
The p38α mitogen-activated protein kinase (MAPK) is activated through stress stimuli such as heat shock or hypoxia. In the nucleus, p38α modulates the activity of other kinases and transcription factors, a process that regulates the expression of specific target genes, most importantly pro-inflammatory cytokines. Dysregulation of p38α therefore plays a major role in the development of inflammatory diseases such as rheumatoid arthritis. Despite many years of intensive research, no p38 small-molecule inhibitors have been approved yet. Several inhibitor design strategies have been reported, leading to >100-fold selective compounds for α/β over the γ and δ isoforms. Achieving such a selectivity among the two structurally most related α and β isoforms, however, remains a challenging task. Targeting an inactive DFG-out conformation offers another strategy for the development of potent kinase inhibitors (type-II), exemplified by the BCR/ABL-inhibitor Imatinib. Achieving selectivity with type-II binders is challenging, because many kinases can adopt an inactive DFG-out conformation. This is exemplified by the p38 type-II inhibitor BIRB-796, which exhibits picomolar on-target affinity but only a poor kinome-wide selectivity. A potent and selective type-II chemical probe for p38α/β was still lacking at the start of this thesis.
The promising hit VPC-00628, was chosen for a combinatorial synthetic approach to develop a type-II chemical probe. The studies covered the optimization of the hinge-binding head group, the hydrophobic region I and the DFG-out deep pocket of the lead compound VPC-00628. Selectivity for the p38α and p38β isoforms was monitored during the optimization process, which identified several inhibitors with favorable isoform selectivity, providing valuable insights into the potential of isoform-selective inhibitor design for p38. A potent and highly selective p38 MAPK probe (SR-318) was discovered, which showed IC50 values in the low nanomolar range in HEK293T cells. An unusual P-loop conformation induced upon binding of SR-318 to p38α contributed most likely to the impressive selectivity profile within the kinome that surpassed both the parent compound and BIRB-796. A negative control compound, SR-321, was developed, to distinguish between on-target effects and non-specific effects due to cross-reactivity with other cellular proteins. Studies of the metabolic stability in human liver microsomes revealed a high stability of the compounds, with only a small amount of metabolites formed over several hours. Compound SR-318 also exhibited a good in vitro efficacy, quantitatively reducing the LPS-stimulated TNF-α release in whole blood. Taken together, SR-318 is a highly potent and selective type-II p38α/β chemical probe, which will help to gain a better understanding of the catalytic and non-catalytic functions of these key signaling kinases in physiology and pathology.
The next studies focused on the exploration of the highly dynamic allosteric back pocket of p38 MAPK, and allosteric BIRB-796 derived compounds for targeting the αC- and DFG-out pockets were synthesized. Kinase activities of allosteric pyrazole-urea fragments were analyzed against a comprehensive set of 47 diverse kinases by differential scanning fluorimetry (DSF), revealing that BIRB-796 off-targets remain a problem when targeting this back-pocket binding motif. Revisiting the recently published compound MCP-081, which combines the allosteric part of BIRB-796 with the active-site directed part of VPC-00628, showed that it displays a clean selectivity profile in our kinase panel. Because the potency of MCP-081 was slightly reduced compared with VPC-00628 and the allosteric tert-butyl pyrazole moiety seemed suboptimal, a set of VPC-00628 derivatives for targeting the αC-out pocket region was synthesized. Through structure-guided extension of the terminal amide of VPC-00628 toward this allosteric site, the potent and selective compound SR-43 was developed, which showed excellent cellular activity on p38 MAPK in NanoBRETTM assays (IC50 [p38α/β] = 14.0 ± 0.1/ 16.8 ± 0.1 nM). SR-43 showed a dose-dependent inhibition of activating phosphorylation of p38 in HCT-15 cells as well as inhibition of phosphorylation of p38 downstream substrates MK2 and Hsp27. In addition, SR-43 induced an anti-inflammatory response by blocking TNF-α release in whole blood and displayed a high metabolic stability. Selectivity profiling of SR-43 revealed a narrow selectivity for additional targets such as the discoidin domain receptor kinases (DDR1/2). DDR kinases play a central role in fibrotic disorders, such as renal and pulmonale fibrosis, atherosclerosis and different forms of cancer. Since selective and potent inhibitors for these important therapeutic targets are largely lacking and the existing inhibitors are of low scaffold diversity, the next study focused on the optimization of SR-43 toward DDR1/2 kinase inhibition. The synthetic work covered the optimization of the hinge-binding head group and the allosteric part of SR-43 toward DDR1/2 kinase inhibition. These studies provided novel insights into the P-loop folding process of p38 MAPK and how targeting of non-conserved amino acids affects inhibitor selectivity. Importantly, they led to the development of a selective dual DDR/p38 inhibitor probe, SR-302, with picomolar affinity for DDR2. SR-302 was efficient in vitro and showed a destabilizing effect on the surface adhesion protein E-cadherin in epithelial cells. In summary, SR-302 and its negative control SR-301 provide a valuable tool set for studying the phenotypic effects of DDR1/2 signaling, e.g., in cancer cell lines.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape, followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
The Born cross sections for the process e+e−→η′π+π− at different center-of-mass energies between 2.00 and 3.08~GeV are reported with improved precision from an analysis of data samples collected with the BESIII detector operating at the BEPCII storage ring. An obvious structure is observed in the Born cross section line shape. Fit as a Breit-Wigner resonance, it has a statistical significance of 6.3σ and a mass and width of M=(2108±46±25)~MeV/c2 and Γ=(138±36±30)~MeV, where the uncertainties are statistical and systematic, respectively. These measured resonance parameters agree with the measurements of BABAR in e+e−→η′π+π− and BESIII in e+e−→ωπ0 within two standard deviations.
Ten hadronic final states of the ℎ𝑐 decays are investigated via the process 𝜓(3686)→𝜋0ℎ𝑐, using a data sample of (448.1±2.9)×106 𝜓(3686) events collected with the BESIII detector. The decay channel ℎ𝑐→𝐾+𝐾−𝜋+𝜋−𝜋0 is observed for the first time and has a measured significance of 6.0𝜎. The corresponding branching fraction is determined to be ℬ(ℎ𝑐→𝐾+𝐾−𝜋+𝜋−𝜋0)=(3.3±0.6±0.6)×10−3 (where the uncertainties are statistical and systematic, respectively). Evidence for the decays ℎ𝑐→𝜋+𝜋−𝜋0𝜂 and ℎ𝑐→𝐾0𝑆𝐾±𝜋∓𝜋+𝜋− is found with a significance of 3.6𝜎 and 3.8𝜎, respectively. The corresponding branching fractions (and upper limits) are obtained to be ℬ(ℎ𝑐→𝜋+𝜋−𝜋0𝜂)=(7.2±1.8±1.3)×10−3 (<1.8×10−2) and ℬ(ℎ𝑐→𝐾0𝑆𝐾±𝜋∓𝜋+𝜋−)=(2.8±0.9±0.5)×10−3 (<4.7×10−3). Upper limits on the branching fractions for the final states ℎ𝑐→𝐾+𝐾−𝜋0, 𝐾+𝐾−𝜂, 𝐾+𝐾−𝜋+𝜋−𝜂, 2(𝐾+𝐾−)𝜋0, 𝐾+𝐾−𝜋0𝜂, 𝐾0𝑆𝐾±𝜋∓, and 𝑝¯𝑝𝜋0𝜋0 are determined at a confidence level of 90%.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape,
followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
Selectivity remains a challenge for ATP-mimetic kinase inhibitors, an issue that may be overcome by targeting unique residues or binding pockets. However, to date only few strategies have been developed. Here we identify that bulky residues located N-terminal to the DFG motif (DFG-1) represent an opportunity for designing highly selective inhibitors with unexpected binding modes. We demonstrate that several diverse inhibitors exerted selective, noncanonical binding modes that exclusively target large hydrophobic DFG-1 residues present in many kinases including PIM, CK1, DAPK, and CLK. By use of the CLK family as a model, structural and biochemical data revealed that the DFG-1 valine controlled a noncanonical binding mode in CLK1, providing a rationale for selectivity over the closely related CLK3 which harbors a smaller DFG-1 alanine. Our data suggest that targeting the restricted back pocket in the small fraction of kinases that harbor bulky DFG-1 residues offers a versatile selectivity filter for inhibitor design.
The FUBP1-FUSE complex is an essential component of a transcription molecular machinery that is necessary for tight regulation of expression of many key genes including c-Myc and p21. FUBP1 utilizes its four articulated KH modules, which function cooperatively, for FUSE nucleotide binding. To understand molecular mechanisms fundamental to the intermolecular interaction, we present a set of crystal structures, as well ssDNA-binding characterization of FUBP1 KH domains. All KH1-4 motifs were highly topologically conserved, and were able to interact with FUSE individually and independently. Nevertheless, differences in nucleotide binding properties among the four KH domains were evident, including higher nucleotide-binding potency for KH3 as well as diverse nucleotide sequence preferences. Variations in amino acid compositions at one side of the binding cleft responsible for nucleobase resulted in diverse shapes and electrostatic charge interaction, which might feasibly be a contributing factor for different nucleotide-binding propensities among KH1-4. Nonetheless, conservation of structure and nucleotide-binding property in all four KH motifs is essential for the cooperativity of multi KH modules present in FUBP1 towards nanomolar affinity for FUSE interaction. Comprehensive structural comparison and ssDNA binding characteristics of all four KH domains presented here provide molecular insights at a fundamental level that might be beneficial for elucidating the mechanisms of the FUBP1-FUSE interaction.
Human protein kinases play essential roles in cellular signaling pathways and - if deregulated - are linked to a large diversity of diseases such as cancer and inflammation or to metabolic diseases. Because of their key role in disease development or progression, kinases have developed into major drug targets resulting in the approval of 52 kinase inhibitors by the Food and Drug Administration (FDA) so far.
Within the drug discovery process, the affinity of the inhibitors is the parameter that is used most often to predict the later efficacy in humans. However, the kinetics of binding have recently emerged as an important but largely neglected factor of kinase inhibitor efficacy. To efficiently suppress a signaling pathway, the targeted kinase needs to be continuously inhibited. Thus, it has been hypothesized that fast binding on-rates and slow off-rates would be the preferred property of an efficacious inhibitor. Despite optimizing the potency of kinase inhibitors, in the past decade optimization of kinetic selectivity has therefore gained interest as a molecule cannot be active unless it is bound, as Paul Ehrlich once stated. There is increasing evidence of correlations between prolonged drug-target residence time and increased drug efficacy, and that inhibitor selectivity in cellular contexts can be modulated by altered residence times. In order to contribute to the understanding of the effect of long residence times on cellular targets we initiated two projects.
The first of these projects is related to the STE20 kinase Serine/threonine kinase 10 (STK10) and its close relative STE20 like kinase (SLK) which have been reported to be frequent off-targets for kinase inhibitors used in the clinics. Also, an inhibition of STK10 and SLK has been linked to a common side-effect of severe skin rash developed upon treatment with the EGFR inhibitor erlotinib, but not gefitinib and the severity of this rash correlated with the treatment outcome, which fits the known biology of STK10 and SLK to be regulators of lymphocyte migration and PLK kinases. However, there are yet no explanations why these two proteins show such high hit-rates across the kinome among the kinase inhibitors. Using structural analysis, we identified the flexibility of STK10 to be the main reason for this hit-rate. The observed strong in vitro potencies did however not translate to the cellular system which is why we investigated the inhibitors residence time on STK10. We found the same flexibility to be the main reason for slow residence times among several inhibitors. We observed large rearrangements in the hydrophobic backpocket of STK10 including the αC, the P-loop enclosing the inhibitor like a lid and strong π-π-stackings to be the main reasons for prolonged residence times on STK10. Interestingly, we observed an increased residence time for erlotinib, which showed skin-related side-effects, giving rise whether the binding kinetics should be investigated for weak cellular off-target effects in future drug discovery efforts.
In the second project we initiated, we illuminate a structural mechanism that allows kinetic selection between two closely related kinases, focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2). Using an inhibitor series designed to probe the mechanism, residence times measured in vitro and in cells showed a strong correlation. Crystal structures and mutagenesis identified hydrophobic interactions with L567, adjacent to the DFG-motif, as being crucial to kinetic selectivity of FAK over PYK2. This specific interaction was observed only when the DFG-motif was stabilized into a helical conformation upon ligand binding to FAK. The interplay between the protein structural mobility and ligand-induced effect was found to be the key regulator of kinetic inhibitor selectivity for FAK over PYK2.
These two projects showed that the parameter residence time should be considered for different problems among the drug discovery process. First, in an open in vivo system not only the potency of a drug alone, but as well its residence time might be of importance. Here we showed that the weak cellular potency translated to prolonged residence times for several inhibitors in cells and established a link between the phenotypic outcome of skin rash after erlotinib treatment and the residence time of this inhibitor on STK10 in cells. On the other hand, medicinal chemistry efforts should consider structure kinetic relationships (SKR) in the optimization process and aim to understand the molecular basis for prolonged target residence times. Here, we showed that a hydrophobic interaction that is enforced upon inhibitor binding is crucial for an unusual helical DFG conformation which arrests the inhibitor and prolongs its residence time providing the molecular basis for understanding the kinetic selectivity of two closely related protein kinases. Establishing the SKRs will help medicinal chemists to kinetically optimize their drug candidates to select a suitable molecule to proceed into further optimization programs. Hence, the projects showed that the target residence time parameter needs to be considered both as a molecular optimization parameter to improve compound potency and binding behavior as well as a parameter to be understood for proceeding to the open system of in vivo models to later modulate the in vivo efficacy of protein kinase targeting drugs.
Nuclear receptor related 1 (Nurr1) is an orphan ligand-activated transcription factor and considered as neuroprotective transcriptional regulator with great potential as therapeutic target for neurodegenerative diseases. However, the collection of available Nurr1 modulators and mechanistic understanding of Nurr1 are limited. Here, we report the discovery of several structurally diverse non-steroidal anti-inflammatory drugs as inverse Nurr1 agonists demonstrating that Nurr1 activity can be regulated bidirectionally. As chemical tools, these ligands enable unraveling the co-regulatory network of Nurr1 and the mode of action distinguishing agonists from inverse agonists. In addition to its ability to dimerize, we observe an ability of Nurr1 to recruit several canonical nuclear receptor co-regulators in a ligand-dependent fashion. Distinct dimerization states and co-regulator interaction patterns arise as discriminating factors of Nurr1 agonists and inverse agonists. Our results contribute a valuable collection of Nurr1 modulators and relevant mechanistic insights for future Nurr1 target validation and drug discovery.
MKK7 (MEK7) is a key regulator of the JNK stress signaling pathway and targeting MKK7 has been proposed as a chemotherapeutic strategy. Detailed understanding of the MKK7 structure and factors that impact its activity is therefore of critical importance. Here, we present a comprehensive set of MKK7 crystal structures revealing insights into catalytic domain plasticity and the role of the N-terminal regulatory helix, conserved in all MAP2Ks, mediating kinase activation. Crystal structures harboring this regulatory helix revealed typical structural features of active kinase, providing exclusively a first model of the MAP2K active state. A small molecule screening campaign yielded multiple scaffolds, including type-II irreversible inhibitors a binding mode that has not been reported previously. We also observed an unprecedented allosteric pocket located in the N-terminal lobe for the approved drug ibrutinib. Collectively, our structural and functional data expand and provide alternative targeting strategies for this important MAP2K kinase.
Unc-51-like kinase 4 (ULK4) is a pseudokinase that has been linked to the development of several diseases. Even though sequence motifs required for ATP binding in kinases are lacking, ULK4 still tightly binds ATP and the presence of the cofactor is required for structural stability of ULK4. Here we present a high-resolution structure of a ULK4-ATPγS complex revealing a highly unusual ATP binding mode in which the lack of the canonical VAIK motif lysine is compensated by K39, located N-terminal to αC. Evolutionary analysis suggests that degradation of active site motifs in metazoan ULK4 has co-occurred with an ULK4 specific activation loop, which stabilizes the C-helix. In addition, cellular interaction studies using BioID and biochemical validation data revealed high confidence interactors of the pseudokinase and armadillo repeat domains. Many of the identified ULK4 interaction partners were centrosomal and tubulin associated proteins and several active kinases suggesting new roles for ULK4.
Highlights: Structure of the ULK4 ATP complex reveals a unique ATP binding mode.
Disease associated mutations modulate ATP binding and ULK4 stability
Degradation of active site motifs co-occurred in evolution with an ULK4 specific activation loop
BioID suggests a role of ULK4 regulating centrosomal and cytoskeletal functions,
Background: To assess late toxicity, quality of life and oncological outcome after consolidative whole abdominal radiotherapy (WART) following cytoreductive surgery and carboplatin/paclitaxel chemotherapy in high risk patients with advanced ovarian cancer FIGO stage III using IMRT (Intensity modulated radiation therapy).
Methods: The OVAR-IMRT-02 study is a multi-center single-arm phase-II-trial. Twenty patients with optimally debulked ovarian cancer stage FIGO III with complete remission after chemotherapy were treated with intensity modulated WART. A total dose of 30 Gy in 20 fractions was applied to the entire peritoneal cavity. Primary endpoint was treatment tolerability; secondary objectives were acute and chronic toxicities, quality of life, rates of therapy disruption/abortion, progression-free survival (PFS) and overall survival (OS).
Results: All patients completed treatment and 10/20 patients (50%) reached the final study follow-up of 36 months. Late side effects consisted of °1-°2 lower limb edema (44.5%), with one patient (5.6%) showing °3 edema. Three patients (16.7%) showed elevated gamma-Glutamyltransferase. There were no severe late side effects regarding
renal or hepatic function or any gastrointestinal toxicity greater than °2. During WART, mean global health status
decreased by 18.1 points (95%-CI: 7.1–29.0), but completely normalized after 6 months. The same trend was observed for the function scale scores. Kaplan-Meier-estimated 1-, 2- and 3-year PFS was 74, 51 and 40%, respectively. 1-, 2- and 3-year OS was 89, 83 and 83%, respectively.
Conclusions: Intensity modulated WART after aggressive surgery and carboplatin/paclitaxel chemotherapy is associated with an acceptable risk of acute and late toxicity and minor impact on long-term quality of life. Together
with the promising results for PFS and OS, intensity modulated WART could offer a new therapeutic option for consolidation treatment of patients with advanced ovarian cancer.
Trial registration: The study is registered with ClinicalTrials.gov (NCT01180504). Registered 12 August 2010 – retrospectively registered.
Digital spatial processes have been widely explored and investigated in subject-specific geographic research. So far, however, this research has not been sufficiently reflected in classrooms or teacher education, and remains unconnected to notions of geographical digital literacy. Viral constructions of space – realities shaped in everyday life that are experienced and (re-)produced by students and teachers alike through social media – present an opportunity for Geography education to adapt to the digital society. This paper attempts to connect viral constructions of space, the digital society and the knowledge teachers need to include viral constructions of space in the classroom using Mishra and Koehler’s (2006) TPACK model, a well-established means for summarizing teachers’ technological, pedagogical and content knowledge for a specific topic. The paper focuses on content knowledge, identifies five sub-types of viral constructions of space, and extracts nine descriptors of teachers’ content knowledge. By focusing on content knowledge, the paper presents a starting point for future investigations of pedagogical and technological teacher knowledge as well as their intersections. It also raises awareness of viral constructions of space as both a new essential topic in the Geography classroom and a phenomenon already shaping learning environments for spatial acquisition.
Using 2.93 fb−1 of 𝑒+𝑒− collision data taken at a center-of-mass energy of 3.773 GeV by the BESIII detector at the BEPCII, we measure the branching fractions of the singly Cabibbo-suppressed decays 𝐷→𝜔𝜋𝜋 to be ℬ(𝐷0→𝜔𝜋+𝜋−)=(1.33±0.16±0.12)×10−3 and ℬ(𝐷+→𝜔𝜋+𝜋0)=(3.87±0.83±0.25)×10−3, where the first uncertainties are statistical and the second ones systematic. The statistical significances are 12.9𝜎 and 7.7𝜎, respectively. The precision of ℬ(𝐷0→𝜔𝜋+𝜋−) is improved by a factor of 2.1 over prior measurements, and ℬ(𝐷+→𝜔𝜋+𝜋0) is measured for the first time. No significant signal for 𝐷0→𝜔𝜋0𝜋0 is observed, and the upper limit on the branching fraction is ℬ(𝐷0→𝜔𝜋0𝜋0)<1.10×10−3 at the 90% confidence level. The branching fractions of 𝐷→𝜂𝜋𝜋 are also measured and consistent with existing results.
Using 2.93 fb−1 of 𝑒+𝑒− collision data taken at a center-of-mass energy of 3.773 GeV with the BESIII detector, we report the first measurements of the absolute branching fractions of 14 hadronic 𝐷0(+) decays to exclusive final states with an 𝜂, e.g., 𝐷0→𝐾−𝜋+𝜂, 𝐾0𝑆𝜋0𝜂, 𝐾+𝐾−𝜂, 𝐾0𝑆𝐾0𝑆𝜂, 𝐾−𝜋+𝜋0𝜂, 𝐾0𝑆𝜋+𝜋−𝜂, 𝐾0𝑆𝜋0𝜋0𝜂, and 𝜋+𝜋−𝜋0𝜂; 𝐷+→𝐾0𝑆𝜋+𝜂, 𝐾0𝑆𝐾+𝜂, 𝐾−𝜋+𝜋+𝜂, 𝐾0𝑆𝜋+𝜋0𝜂, 𝜋+𝜋+𝜋−𝜂, and 𝜋+𝜋0𝜋0𝜂. Among these decays, the 𝐷0→𝐾−𝜋+𝜂 and 𝐷+→𝐾0 𝑆𝜋+𝜂 decays have the largest branching fractions, which are ℬ(𝐷0→𝐾−𝜋+𝜂) = (1.853±0.025stat±0.031syst)% and ℬ(𝐷+→𝐾0𝑆𝜋+𝜂) = (1.309±0.037stat±0.031syst)%, respectively. The charge-parity asymmetries for the six decays with highest event yields are determined, and no statistically significant charge-parity violation is found.
Background: Naturalistic developmental behavioural interventions (NDBI) have been shown to improve autism-specific symptoms in young children with Autism Spectrum Disorder (ASD). NDBI approaches, such as the ASD-specific Frankfurt Early Intervention Programme for ASD (A-FFIP), are based on ASD-specific developmental and learning aspects. A-FFIP is a low-intensity intervention which can easily be implemented in the local health care/social welfare system. The aim of the present study is to establish 1-year efficacy of the manualised early intervention programme A-FFIP in toddlers and preschool children with ASD. It is hypothesised that A-FFIP will result in improved ASD-specific symptoms compared to early intervention as usual (EIAU). Child- and family-specific secondary outcomes, as well as moderators and mediators of outcome, will be explored.
Methods/design: A prospective, multi-centre, parallel-group, randomised controlled, phase-III trial comparing A-FFIP versus EIAU. A total of 134 children (A-FFIP: 67, EIAU: 67) aged 24–66 months at baseline assessment meeting the criteria for ASD (DSM-5) will be included. The primary outcome is the absolute change of the total score of the Brief Observation of Social Communication Change (BOSCC-AT) between baseline (T2) and 1-year follow-up (T6). The treatment effect will be tested, adjusted for relevant covariates applying a mixed model for repeated measures. Secondary outcomes are BOSCC social communication and repetitive-behaviour scores, single ASD symptoms, language, cognition, psychopathology, parental well-being and family quality of life. Predictors, moderators and mediating mechanisms will be explored.
Discussion: If efficacy of the manualised A-FFIP early intervention is established, the current study has the potential to change clinical practice strongly towards the implementation of a low-intensity, evidence-based, natural early intervention in ASD. Early intervention in ASD requires specialist training, which subsequently needs to be developed or included into current training curricula.
Trial registration: German Registry for Clinical Trials (Deutscher Register Klinischer Studien, DRKS); ID: 00016330. Retrospectively registered on 4 January 2019. URL: https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00016330.
Cross sections of the process 𝑒+𝑒−→𝜋0𝜋0𝐽/𝜓 at center-of-mass energies between 3.808 and 4.600 GeV are measured with high precision by using 12.4 fb−1 of data samples collected with the BESIII detector operating at the BEPCII collider facility. A fit to the measured energy-dependent cross sections confirms the existence of the charmoniumlike state 𝑌(4220). The mass and width of the 𝑌(4220) are determined to be (4220.4±2.4±2.3) MeV/𝑐2 and (46.2±4.7±2.1) MeV, respectively, where the first uncertainties are statistical and the second systematic. The mass and width are consistent with those measured in the process 𝑒+𝑒−→𝜋+𝜋−𝐽/𝜓. The neutral charmonium-like state 𝑍𝑐(3900)0 is observed prominently in the 𝜋0𝐽/𝜓 invariant-mass spectrum, and, for the first time, an amplitude analysis is performed to study its properties. The spin-parity of 𝑍𝑐(3900)0 is determined to be 𝐽𝑃=1+, and the pole position is (3893.1±2.2±3.0)−𝑖(22.2±2.6±7.0) MeV/𝑐2, which is consistent with previous studies of electrically charged 𝑍𝑐(3900)±. In addition, cross sections of 𝑒+𝑒− → 𝜋0𝑍𝑐(3900)0 → 𝜋0𝜋0𝐽/𝜓 are extracted, and the corresponding line shape is found to agree with that of the 𝑌(4220).
Plants, fungi and algae are important components of global biodiversity and are fundamental to all ecosystems. They are the basis for human well-being, providing food, materials and medicines. Specimens of all three groups of organisms are accommodated in herbaria, where they are commonly referred to as botanical specimens.The large number of specimens in herbaria provides an ample, permanent and continuously improving knowledge base on these organisms and an indispensable source for the analysis of the distribution of species in space and time critical for current and future research relating to global biodiversity. In order to make full use of this resource, a research infrastructure has to be built that grants comprehensive and free access to the information in herbaria and botanical collections in general. This can be achieved through digitization of the botanical objects and associated data.The botanical research community can count on a long-standing tradition of collaboration among institutions and individuals. It agreed on data standards and standard services even before the advent of computerization and information networking, an example being the Index Herbariorum as a global registry of herbaria helping towards the unique identification of specimens cited in the literature.In the spirit of this collaborative history, 51 representatives from 30 institutions advocate to start the digitization of botanical collections with the overall wall-to-wall digitization of the flat objects stored in German herbaria. Germany has 70 herbaria holding almost 23 million specimens according to a national survey carried out in 2019. 87% of these specimens are not yet digitized. Experiences from other countries like France, the Netherlands, Finland, the US and Australia show that herbaria can be comprehensively and cost-efficiently digitized in a relatively short time due to established workflows and protocols for the high-throughput digitization of flat objects.Most of the herbaria are part of a university (34), fewer belong to municipal museums (10) or state museums (8), six herbaria belong to institutions also supported by federal funds such as Leibniz institutes, and four belong to non-governmental organizations. A common data infrastructure must therefore integrate different kinds of institutions.Making full use of the data gained by digitization requires the set-up of a digital infrastructure for storage, archiving, content indexing and networking as well as standardized access for the scientific use of digital objects. A standards-based portfolio of technical components has already been developed and successfully tested by the Biodiversity Informatics Community over the last two decades, comprising among others access protocols, collection databases, portals, tools for semantic enrichment and annotation, international networking, storage and archiving in accordance with international standards. This was achieved through the funding by national and international programs and initiatives, which also paved the road for the German contribution to the Global Biodiversity Information Facility (GBIF).Herbaria constitute a large part of the German botanical collections that also comprise living collections in botanical gardens and seed banks, DNA- and tissue samples, specimens preserved in fluids or on microscope slides and more. Once the herbaria are digitized, these resources can be integrated, adding to the value of the overall research infrastructure. The community has agreed on tasks that are shared between the herbaria, as the German GBIF model already successfully demonstrates.We have compiled nine scientific use cases of immediate societal relevance for an integrated infrastructure of botanical collections. They address accelerated biodiversity discovery and research, biomonitoring and conservation planning, biodiversity modelling, the generation of trait information, automated image recognition by artificial intelligence, automated pathogen detection, contextualization by interlinking objects, enabling provenance research, as well as education, outreach and citizen science.We propose to start this initiative now in order to valorize German botanical collections as a vital part of a worldwide biodiversity data pool.
Digitale Technologien begünstigen den Einsatz einer dynamischen Preisgestaltung, also von Preisen, die für ein prinzipiell gleiches Produkt unangekündigt variieren. Dabei werden in der öffentlichen Diskussion unterschiedliche Ausgestaltungsformen dynamischer Preise oftmals vermischt, was eine sinnvolle Analyse der Vor- und Nachteile der dynamischen Preisgestaltung erschwert. Das Ziel des Beitrags ist die Darstellung der ökonomischen Grundlagen und die Diskussion sowie Klassifikation der Ausgestaltungsmöglichkeiten der dynamischen Preisgestaltung. Darüber hinaus erfolgt eine Bewertung der Vor- und Nachteile der dynamischen Preisgestaltung aus Käufer- und Verkäufersicht. Abschließend werden Implikationen für die betriebswirtschaftliche Forschung diskutiert.