Refine
Year of publication
Document Type
- Article (87)
- Contribution to a Periodical (4)
- Preprint (2)
- Part of a Book (1)
Has Fulltext
- yes (94)
Is part of the Bibliography
- no (94)
Keywords
- NMR spectroscopy (14)
- SARS-CoV-2 (11)
- RNA (10)
- COVID19-NMR (5)
- G-quadruplexes (4)
- NMR (4)
- Solution NMR spectroscopy (4)
- Solution NMR-spectroscopy (4)
- rna (4)
- structural biology (4)
- 5′-UTR (3)
- Covid19-NMR (3)
- Mycobacterium tuberculosis (3)
- Non-structural protein (3)
- Protein drugability (2)
- RNA structures (2)
- aptamers (2)
- base pairing (2)
- biophysics (2)
- heteronuclear detection (2)
- kinetics (2)
- nuclear magnetic resonance spectroscopy (2)
- proteins (2)
- proteomics (2)
- reactive oxygen species (2)
- real-time NMR spectroscopy (2)
- small protein (2)
- small proteins (2)
- structure elucidation (2)
- 19F (1)
- 19F MR spectroscopy (1)
- 1H MR spectroscopy (1)
- 2'-deoxyguanosine riboswitch (1)
- 2-hydroxyglutarate (1)
- 2D NMR spectroscopy (1)
- 5'-UTR (1)
- 5_SL4 (1)
- ATG3 (1)
- B. subtilis (1)
- Bacterial Protein Kinases (1)
- Bacterial Protein Phosphatases (1)
- Biochemie (1)
- Biotin (1)
- Bradyrhizobium (1)
- C-mannosylation (1)
- CEST (1)
- COVID-19 (1)
- Covid19-nmr (1)
- DNA (1)
- DNA-PAINT (1)
- DNA-ligand complexes (1)
- Dimerization domain (1)
- Direct carbon (1)
- Drug Resistance (1)
- Drug discovery (1)
- Dynamische Kernpolarisation (1)
- E. coli (1)
- Echtzeit-NMR-Spektroskopie (1)
- Empfindlichkeitsverstärkung (1)
- Eph receptors (1)
- Ephrin ligand (1)
- Esters (1)
- Eukaryota (1)
- FBDD (1)
- FBS (1)
- FGFR (1)
- Fragment (1)
- G-protein-coupled receptors (1)
- G-quadruplex binders (1)
- Haloferax volcanii (1)
- HeLa cells (1)
- High-throughput screening (1)
- Hohes Magnetfeld (1)
- IDH mutation (1)
- IDH1 inhibitor (1)
- Internal ribosome entry site (1)
- Ligands (1)
- Low Molecular Weight PTP (1)
- Luciferase (1)
- Macrodomain (1)
- Methanosarcina mazei (1)
- Molecular modelling (1)
- MptpA (1)
- NMR Spectroscopy (1)
- NMR solution structure (1)
- NMR-Spektroskopie (1)
- NOESY (1)
- Nuclear magnetic resonance (1)
- Nucleic acid-binding domain (1)
- Nucleocapsid (1)
- Personalisierte Medizin (1)
- Phosphorylation (1)
- Primary metabolites (1)
- Protein druggability (1)
- Protein translation (1)
- PtkA (1)
- Quality control (1)
- RNA genome (1)
- RNA sequencing (RNA-Seq) (1)
- RNA stability (1)
- RNA synthesis (1)
- RNA therapy (1)
- RNASolution-state NMR (1)
- SHAPE analysis (1)
- SL1 (1)
- SL5a (1)
- SL5b (1)
- SL5b + c (1)
- SL5c (1)
- SSR128129E (1)
- Secondary metabolites (1)
- Shine-Dalgarno (1)
- Sinorhizobium fredii (1)
- Solubility (1)
- Solution-state NMR (1)
- Soybean (1)
- Stoffwechsel (1)
- Structural protein (1)
- TERRA RNA (1)
- Target validation (1)
- Translation initiation (1)
- UV/Vis spectroscopy (1)
- X-ray diffraction (1)
- Zellstudien (1)
- a-proteobacteria (1)
- accessory proteins (1)
- acute myeloid leukemia (1)
- adenine (1)
- alkylation (1)
- allostery (1)
- amino acids (1)
- analysis (1)
- analytical chemistry (1)
- antibiotics (1)
- autophagy (1)
- autophagy inhibition (1)
- barstar (1)
- biochemistry (1)
- biological chemistry (1)
- biological models (1)
- biophysical investigation (1)
- c-Myc (1)
- carbazole ligands (1)
- carbon direct detection (1)
- cell death (1)
- cell studies (1)
- cell-free protein synthesis (1)
- chemoenzymatic synthesis (1)
- chronic myeloid leukemia (1)
- circular dichroism (1)
- click chemistry (1)
- colorectal cancer (1)
- computational chemistry (1)
- conformation analysis (1)
- cysteine reactivity (1)
- cysteine-redox regulation (1)
- cytochromes (1)
- detection (1)
- diagnostic radiologic examination (1)
- drug design (1)
- entropy (1)
- eph receptor tyrosin kinase family (1)
- ephrins (1)
- fluorescence (1)
- fluorine (1)
- folding (1)
- folding landscapes (1)
- fragment screening (1)
- fragment-based screening (1)
- genetic code expansion (1)
- glioma (1)
- glutamine synthetase regulation (1)
- glutathione (1)
- glutathionylation (1)
- glycoproteins (1)
- guanidine riboswitch (1)
- hydroxynaphthoquinone (1)
- inhibitor (1)
- inhibitor design (1)
- intrinsically disordered protein (1)
- intrinsically disordered region (1)
- ions (1)
- isotope labeling (1)
- large functional RNAs (1)
- ligand design (1)
- ligands (1)
- ligases (1)
- light control (1)
- meta-stable structures (1)
- metabolic reprogramming (1)
- metabolic rewiring (1)
- metabolism (1)
- metals (1)
- molecular conformation (1)
- murine model (1)
- nitrogen direct detection (1)
- nitrogen regulation (1)
- nitroindoles (1)
- nitrosylation (1)
- non-canonical amino acid (1)
- non-natural nucleotide (1)
- nonstructural proteins (1)
- nucleobases (1)
- oligonucleotides (1)
- oncogene promoters (1)
- oxidases (1)
- oxidative folding (1)
- personalized medicine (1)
- photochemistry (1)
- plant symbioses (1)
- plasmid copy number (1)
- precision (1)
- proline isomerization (1)
- protein denaturation (1)
- protein folding (1)
- protein oxidation (1)
- protein phosphorylation (1)
- protein tyrosine kinase (1)
- protein tyrosine phosphatase (1)
- protons (1)
- quorum sensing (QS) (1)
- reductases (1)
- regioisomers (1)
- retinal (1)
- rhodopsin (1)
- ribosomal binding site (1)
- ribosomal exit tunnel (1)
- ribosome (1)
- riboswitches (1)
- ribozymes (1)
- roentgen rays (1)
- sORF (1)
- salmonella (1)
- selective isotopic labeling (1)
- site-specific labeling (1)
- small ORFs (1)
- small gene (1)
- small molecule inhibitor (1)
- solid-phase synthesis (1)
- spectrum (1)
- spectrum analysis (1)
- structural proteins (1)
- structure-activity relationships (1)
- structure–activity relationships (1)
- targeted therapy (1)
- temperature (1)
- temperature jump (1)
- thermometers (1)
- thiostrepton (1)
- transcription (1)
- transient complex (1)
- translation initiation region (1)
- tumor angiogenesis (1)
- tumor hypoxia (1)
- tumor perfusion (1)
- tyrosine kinase inhibitors (1)
- tyrosine kinase inhibitors. (1)
- tyrosine kinase signaling (1)
- zinc finger (1)
- µ-protein (1)
Institute
- Biochemie und Chemie (47)
- Zentrum für Biomolekulare Magnetische Resonanz (BMRZ) (44)
- Biochemie, Chemie und Pharmazie (35)
- Exzellenzcluster Makromolekulare Komplexe (23)
- Sonderforschungsbereiche / Forschungskollegs (23)
- Biowissenschaften (19)
- Medizin (7)
- Präsidium (4)
- Georg-Speyer-Haus (3)
- Frankfurt Institute for Advanced Studies (FIAS) (1)
Long non-coding RNAs are a very versatile class of molecules that can have important roles in regulating a cells function, including regulating other genes on the transcriptional level. One of these mechanisms is that RNA can directly interact with DNA thereby recruiting additional components such as proteins to these sites via an RNA:dsDNA triplex formation. We genetically deleted the triplex forming sequence (FendrrBox) from the lncRNA Fendrr in mice and found that this FendrrBox is partially required for Fendrr function in vivo. We found that the loss of the triplex forming site in developing lungs causes a dysregulation of gene programs associated with lung fibrosis. A set of these genes contain a triplex site directly at their promoter and are expressed in lung fibroblasts. We biophysically confirmed the formation of an RNA:dsDNA triplex with target promoters in vitro. We found that Fendrr with the Wnt signalling pathway regulates these genes, implicating that Fendrr synergizes with Wnt signalling in lung fibrosis.
During evolution of an RNA world, the development of enzymatic function was essential. Such enzymatic function was linked to RNA sequences capable of adopting specific RNA folds that possess catalytic pockets to promote catalysis. Within this primordial RNA world, initially evolved self-replicating ribozymes presumably mutated to ribozymes with new functions. Schultes and Bartel (Science 2000, 289, 448–452) investigated such conversion from one ribozyme to a new ribozyme with distinctly different catalytic functions. Within a neutral network that linked these two prototype ribozymes, a single RNA chain could be identified that exhibited both enzymatic functions. As commented by Schultes and Bartel, this system possessing one sequence with two enzymatic functions serves as a paradigm for an evolutionary system that allows neutral drifts by stepwise mutation from one ribozyme into a different ribozyme without loss of intermittent function. Here, we investigated this complex functional diversification of ancestral ribozymes by analyzing several RNA sequences within this neutral network between two ribozymes with class III ligase activity and with self-cleavage reactivity. We utilized rapid RNA sample preparation for NMR spectroscopic studies together with SHAPE analysis and in-line probing to characterize secondary structure changes within the neutral network. Our investigations allowed delineation of the secondary structure space and by comparison with the previously determined catalytic function allowed correlation of the structure-function relation of ribozyme function in this neutral network.
The Mycobacterium tuberculosis tyrosine-specific phosphatase MptpA and its cognate kinase PtkA are prospective targets for anti-tuberculosis drugs as they interact with the host defense response within the macrophages. Although both are structurally well-characterized, the functional mechanism regulating their activity remains poorly understood. Here, we investigate the effect of post-translational oxidation in regulating the function of MptpA. Treatment of MptpA with H2O2/NaHCO3, mimicking cellular oxidative stress conditions, leads to oxidation of the catalytic cysteine (C11) and to a conformational rearrangement of the phosphorylation loop (D-loop) by repositioning the conserved tyrosine 128 (Y128) and generating a temporarily inactive preclosed state of the phosphatase. Thus, the catalytic cysteine in the P-loop acts as a redox switch and regulates the phosphatase activity of MptpA.
Riboswitches are gene regulatory elements located in untranslated mRNA regions. They bind inducer molecules with high affinity and specificity. Cyclic-di-nucleotide-sensing riboswitches are major regulators of genes for the environment, membranes and motility (GEMM) of bacteria. Up to now, structural probing assays or crystal structures have provided insight into the interaction between cyclic-di-nucleotides and their corresponding riboswitches. ITC analysis, NMR analysis and computational modeling allowed us to gain a detailed understanding of the gene regulation mechanisms for the Cd1 (Clostridium difficile) and for the pilM (Geobacter metallireducens) riboswitches and their respective di-nucleotides c-di-GMP and c-GAMP. Binding capability showed a 25 nucleotide (nt) long window for pilM and a 61 nt window for Cd1. Within this window, binding affinities ranged from 35 μM to 0.25 μM spanning two orders of magnitude for Cd1 and pilM showing a strong dependence on competing riboswitch folds. Experimental results were incorporated into a Markov simulation to further our understanding of the transcriptional folding pathways of riboswitches. Our model showed the ability to predict riboswitch gene regulation and its dependence on transcription speed, pausing and ligand concentration.
Long non-coding RNAs are a very versatile class of molecules that can have important roles in regulating a cells function, including regulating other genes on the transcriptional level. One of these mechanisms is that RNA can directly interact with DNA thereby recruiting additional components such as proteins to these sites via a RNA:dsDNA triplex formation. We genetically deleted the triplex forming sequence (FendrrBox) from the lncRNA Fendrr in mice and find that this FendrrBox is partially required for Fendrr function in vivo. We find that the loss of the triplex forming site in developing lungs causes a dysregulation of gene programs, associated with lung fibrosis. A set of these genes contain a triplex site directly at their promoter and are expressed in fibroblasts. We confirm the formation of RNA:dsDNA formation with target promoters. We find that Fendrr with the Wnt signalling pathway regulates these genes, implicating that Fendrr synergizes with Wnt signalling in lung fibrosis.
1H, 13C and 15N chemical shift assignment of the stem-loops 5b + c from the 5′-UTR of SARS-CoV-2
(2022)
The ongoing pandemic of the respiratory disease COVID-19 is caused by the SARS-CoV-2 (SCoV2) virus. SCoV2 is a member of the Betacoronavirus genus. The 30 kb positive sense, single stranded RNA genome of SCoV2 features 5′- and 3′-genomic ends that are highly conserved among Betacoronaviruses. These genomic ends contain structured cis-acting RNA elements, which are involved in the regulation of viral replication and translation. Structural information about these potential antiviral drug targets supports the development of novel classes of therapeutics against COVID-19. The highly conserved branched stem-loop 5 (SL5) found within the 5′-untranslated region (5′-UTR) consists of a basal stem and three stem-loops, namely SL5a, SL5b and SL5c. Both, SL5a and SL5b feature a 5′-UUUCGU-3′ hexaloop that is also found among Alphacoronaviruses. Here, we report the extensive 1H, 13C and 15N resonance assignment of the 37 nucleotides (nts) long sequence spanning SL5b and SL5c (SL5b + c), as basis for further in-depth structural studies by solution NMR spectroscopy.
The ribosomal S1 protein (rS1) is indispensable for translation initiation in Gram-negative bacteria. rS1 is a multidomain protein that acts as an RNA chaperone and ensures that mRNAs can bind the ribosome in a single-stranded conformation, which could be related to fast recognition. Although many ribosome structures were solved in recent years, a high-resolution structure of a two-domain mRNA-binding competent rS1 construct is not yet available. Here, we present the NMR solution structure of the minimal mRNA-binding fragment of Vibrio Vulnificus rS1 containing the domains D3 and D4. Both domains are homologues and adapt an oligonucleotide-binding fold (OB fold) motif. NMR titration experiments reveal that recognition of miscellaneous mRNAs occurs via a continuous interaction surface to one side of these structurally linked domains. Using a novel paramagnetic relaxation enhancement (PRE) approach and exploring different spin-labeling positions within RNA, we were able to track the location and determine the orientation of the RNA in the rS1–D34 bound form. Our investigations show that paramagnetically labeled RNAs, spiked into unmodified RNA, can be used as a molecular ruler to provide structural information on protein-RNA complexes. The dynamic interaction occurs on a defined binding groove spanning both domains with identical β2-β3-β5 interfaces. Evidently, the 3′-ends of the cis-acting RNAs are positioned in the direction of the N-terminus of the rS1 protein, thus towards the 30S binding site and adopt a conformation required for translation initiation.
Polymorphic G-quadruplex (G4) secondary DNA structures have received increasing attention in medicinal chemistry owing to their key involvement in the regulation of the maintenance of genomic stability, telomere length homeostasis and transcription of important proto-oncogenes. Different classes of G4 ligands have been developed for the potential treatment of several human diseases. Among them, the carbazole scaffold with appropriate side chain appendages has attracted much interest for designing G4 ligands. Because of its large and rigid π-conjugation system and ease of functionalization at three different positions, a variety of carbazole derivatives have been synthesized from various natural or synthetic sources for potential applications in G4-based therapeutics and biosensors. Herein, we provide an updated close-up of the literatures on carbazole-based G4 ligands with particular focus given on their detailed binding insights studied by NMR spectroscopy. The structure-activity relationships and the opportunities and challenges of their potential applications as biosensors and therapeutics are also discussed. This review will provide an overall picture of carbazole ligands with remarkable G4 topological preference, fluorescence properties and significant bioactivity; portraying carbazole as a very promising scaffold for assembling G4 ligands with a range of novel functional applications.
Riboswitches are regulatory RNA elements that undergo functionally important allosteric conformational switching upon binding of specific ligands. The here investigated guanidine-II riboswitch binds the small cation, guanidinium, and forms a kissing loop-loop interaction between its P1 and P2 hairpins. We investigated the structural changes to support previous studies regarding the binding mechanism. Using NMR spectroscopy, we confirmed the structure as observed in crystal structures and we characterized the kissing loop interaction upon addition of Mg2+ and ligand for the riboswitch aptamer from Escherichia coli. We further investigated closely related mutant constructs providing further insight into functional differences between the two (different) hairpins P1 and P2. Formation of intermolecular interactions were probed by small-angle X-ray scattering (SAXS) and NMR DOSY data. All data are consistent and show the formation of oligomeric states of the riboswitch induced by Mg2+ and ligand binding.