Refine
Year of publication
- 2002 (1305) (remove)
Document Type
- Article (524)
- Doctoral Thesis (189)
- Part of Periodical (130)
- Part of a Book (100)
- Review (88)
- Working Paper (83)
- Book (50)
- Preprint (47)
- Conference Proceeding (23)
- diplomthesis (22)
Language
- German (890)
- English (362)
- French (19)
- Portuguese (15)
- mis (5)
- Multiple languages (5)
- Spanish (5)
- Turkish (2)
- Italian (1)
- Polish (1)
Keywords
- Rezension (49)
- Deutschland (26)
- Literatur (20)
- Frankfurt <Main> / Universität (17)
- Frankfurt <Main> (16)
- Theater (14)
- Vormärz (14)
- Deutsch (12)
- Phonetik (12)
- Phonologie (11)
Institute
- Physik (85)
- Extern (76)
- Medizin (67)
- Rechtswissenschaft (48)
- Biochemie und Chemie (46)
- Wirtschaftswissenschaften (38)
- Biowissenschaften (32)
- Gesellschaftswissenschaften (31)
- Pharmazie (25)
- Informatik (22)
We investigated the molecular mechanism of cyclic GMP-induced down-regulation of soluble guanylyl cyclase expression in rat aorta. 3-(5′-Hydroxymethyl-2′-furyl)-1-benzyl indazole (YC-1), an allosteric activator of this enzyme, decreased the expression of soluble guanylyl cyclase α1 subunit mRNA and protein. This effect was blocked by the enzyme inhibitor 4H-8-bromo-1,2,4-oxadiazolo(3,4-d)benz(b-1,4)oxazin-1-one (NS2028) and by actinomycin D. Guanylyl cyclase α1mRNA-degrading activity was increased in protein extracts from YC-1-exposed aorta and was attenuated by pretreatment with actinomycin D and NS2028. Gelshift and supershift analyses using an adenylate-uridylate-rich ribonucleotide from the 3′-untranslated region of the α1 mRNA and a monoclonal antibody directed against the mRNA-stabilizing protein HuR revealed HuR mRNA binding activity in aortic extracts, which was absent in extracts from YC-1-stimulated aortas. YC-1 decreased the expression of HuR, and this decrease was prevented by NS2028. Similarly, down-regulation of HuR by RNA interference in cultured rat aortic smooth muscle cells decreased α1 mRNA and protein expression. We conclude that HuR protects the guanylyl cyclase α1 mRNA by binding to the 3′-untranslated region. Activation of guanylyl cyclase decreases HuR expression, inducing a rapid degradation of guanylyl cyclase α1 mRNA and lowering α1 subunit expression as a negative feedback response.
The potential of a protein-engineered His tag to immobilize macromolecules in a predictable orientation at metal-chelating lipid interfaces was investigated using recombinant 20 S proteasomes His-tagged in various positions. Electron micrographs demonstrated that the orientation of proteasomes bound to chelating lipid films could be controlled via the location of their His tags: proteasomes His-tagged at their sides displayed exclusively side-on views, while proteasomes His-tagged at their ends displayed exclusively end-on views. The activity of proteasomes immobilized at chelating lipid interfaces was well preserved. In solution, His-tagged proteasomes hydrolyzed casein at rates comparable with wild-type proteasomes, unless the His tags were located in the vicinity of the N termini of α-subunits. The N termini of α-subunits might partly occlude the entrance channel in α-rings through which substrates enter the proteasome for subsequent degradation. A combination of electron micrographs and atomic force microscope topographs revealed a propensity of vertically oriented proteasomes to crystallize in two dimensions on fluid lipid films. The oriented immobilization of His-tagged proteins at biocompatible lipid interfaces will assist structural studies as well as the investigation of biomolecular interaction via a wide variety of surface-sensitive techniques including single-molecule analysis.
The yeast F1F0-ATP synthase forms dimeric complexes in the mitochondrial inner membrane and in a manner that is supported by the F0-sector subunits, Su e and Su g. Furthermore, it has recently been demonstrated that the binding of the F1F0-ATPase natural inhibitor protein to purified bovine F1-sectors can promote their dimerization in solution (Çabezon, E., Arechaga, I., Jonathan P., Butler, G., and Walker J. E. (2000) J. Biol. Chem. 275, 28353–28355). It was unclear until now whether the binding of the inhibitor protein to the F1 domains contributes to the process of F1F0-ATP synthase dimerization in intact mitochondria. Here we have directly addressed the involvement of the yeast inhibitor protein, Inh1, and its known accessory proteins, Stf1 and Stf2, in the formation of the yeast F1F0-ATP synthase dimer. Using mitochondria isolated from null mutants deficient in Inh1, Stf1, and Stf2, we demonstrate that formation of the F1F0-ATP synthase dimers is not adversely affected by the absence of these proteins. Furthermore, we demonstrate that the F1F0-ATPase monomers present in su e null mutant mitochondria can be as effectively inhibited by Inh1, as its dimeric counterpart in wild-type mitochondria. We conclude that dimerization of the F1F0-ATP synthase complexes involves a physical interaction of the membrane-embedded F0 sectors from two monomeric complexes and in a manner that is independent of inhibitory activity of the Inh1 and accessory proteins.
Possible hadronization of supercooled QGP, created in heavy ion collisions at RHIC and SPS, is discussed within a Bjorken hydrodynamic model. Such a hadronization is expected to be a very fast shock-like process, what, if hadronization coincides or shortly followed by freeze out, could explain a part of the HBT puzzle, i.e., the flash-like particle emission (Rout/Rside≈1). HBT data also show that the expansion time before freeze out is very short (∼6–10 fm/c). In this Letter we discuss the question of supercooled QGP and the timescale of the reaction.
Signal transducer and activator of transcription 6 (STAT6) regulates transcriptional activation in response to interleukin-4 (IL-4)-induced tyrosine phosphorylation by direct interaction with coactivators. The CREB-binding protein and the nuclear coactivator 1 (NCoA-1), a member of the p160/steroid receptor coactivator family, bind independently to specific regions of STAT6 and act as coactivators. In this study we show that an LXXLL motif in the STAT6 transactivation domain mediates the interaction with NCoA-1. Peptides representing this motif as well as antibodies generated against this motif inhibited STAT6/NCoA-1 interaction in glutathione S-transferase pulldown assays. Peptides derived from the STAT6 transactivation domain adjacent to the LXXLL motif as well as antibodies against these peptides showed no inhibitory effect. Mutagenesis of the LXXLL motif eliminated the STAT6/NCoA-1 interaction in vitro and in vivo, supporting the specific role of this motif in NCoA-1 binding. Importantly, mutagenesis of the STAT-LXXLL motif strongly diminished the IL-4-regulated activation of the endogenous STAT6 target gene eotaxin-3. Taken together, these results indicate that the STAT6-LXXLL-binding motif mediates the interaction with NCoA-1 in transcriptional activation and represents a new potential drug target for the inhibition of the STAT6 transactivation function in allergic diseases.
Production of J/ψ mesons in heavy ion collisions is considered within the statistical coalescence model. The model is in agreement with the experimental data of the NA50 Collaboration for Pb+Pb collisions at 158 AGeV in a wide centrality range, including the so-called “anomalous” suppression domain. The model description of the J/ψ data requires, however, strong enhancement of the open charm production in central Pb+Pb collisions. This model prediction may be checked in the future SPS runs.
The measured particle ratios in central heavy-ion collisions at RHIC-BNL are investigated within a chemical and thermal equilibrium chiral SU(3) σ–ω approach. The commonly adopted noninteracting gas calculations yield temperatures close to or above the critical temperature for the chiral phase transition, but without taking into account any interactions. Contrary, the chiral SU(3) model predicts temperature and density dependent effective hadron masses and effective chemical potentials in the medium and a transition to a chirally restored phase at high temperatures or chemical potentials. Three different parametrizations of the model, which show different types of phase transition behaviour, are investigated. We show that if a chiral phase transition occured in those collisions, “freezing” of the relative hadron abundances in the symmetric phase is excluded by the data. Therefore, either very rapid chemical equilibration must occur in the broken phase, or the measured hadron ratios are the outcome of the dynamical symmetry breaking. Furthermore, the extracted chemical freeze-out parameters differ considerably from those obtained in simple noninteracting gas calculations. In particular, the three models yield up to 35 MeV lower temperatures than the free gas approximation. The in-medium masses turn out to differ up to 150 MeV from their vacuum values.
Eine formgeschichtliche Betrachtung kann zeigen, daß in Hebels "Rheinländischem Hausfreund" die narratologische Beziehung zwischen Kalendermann und Leser sich nur scheinbar harmlos und vertraulich darstellt, im Text sich aber als simulierte Nähe aus Distanz und Fremdheit herstellt. Auf vergleichbare Weise wird eine in den Kalendern simulierte Mündlichkeit beschreibbar als Produkt einer um 1800 sich durchsetzenden dominanten Schriftlichkeit. Die formgeschichtliche Analyse der Kalenderfolge kann eine im Schatzkästlein nicht mehr ersichtliche Korrespondenz von Beschreibungen des Kosmos und politischen "Weltbegebenheiten" rekonstruieren und damit eine bislang behauptete statische Geschichtsauffassung widerlegen. Schließlich vermag die formale Analyse einer raffinierten Verschränkung von Satire und Camouflage die in Hebels Reise nach Paris eingeschriebene Distanz sowohl zu den Nationalisten wie zu den regierenden Monarchien herauszuarbeiten.
Naturschutz-Info 2/2002
(2002)
Naturschutz-Info 1/2002
(2002)