Optimization of Structure‐Guided Development of Chemical Probes for the Pseudoknot RNA of the Frameshift Element in SARS‐CoV‐2

Targeting the RNA genome of SARS-CoV-2 is a viable option for antiviral drug development. We explored three ligand binding sites of the core pseudoknot RNA of the SARS-CoV-2 frameshift element. We iteratively optimized ligands, based on improved affinities, targeting these binding sites and report on structural and dynamic properties of the three identified binding sites. Available experimental 3D structures of the pseudoknot element were compared to SAXS and NMR data to validate its dominant folding state in solution. In order to experimentally map in silico predicted binding sites, NMR assignments of the majority of nucleobases were achieved by segmental labeling of the pseudoknot RNA and isotope-filtered NMR experiments at 1.2 GHz, demonstrating the value of NMR spectroscopy to supplement modelling and docking data. Optimized ligands with enhanced affinity were shown to specifically inhibit frameshifting without affecting 0-frame translation in cell-free translation assays, establishing the frameshift element as target for drug-like ligands of low molecular weight.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-01-29
DOI
https://doi.org/10.1002/anie.202417961
Citations
8
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
6.45

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article

Optimization of Structure‐Guided Development of Chemical Probes for the Pseudoknot RNA of the Frameshift Element in SARS‐CoV‐2

Jennifer Adam, Julia E. Weigand, Andreas Schlundt, Christian Richter et al.
8 citations
Angewandte Chemie International Edition
RNA and protein synthesis mechanisms
6.45
article

Optimization of Structure‐Guided Development of Chemical Probes for the Pseudoknot RNA of the Frameshift Element in SARS‐CoV‐2

Jennifer Adam, Julia E. Weigand, Andreas Schlundt, Christian Richter, Neva Caliskan, Harald Schwalbe, Sabrina Toews, Michael Göbel, Anna Wacker, Frank J. Kaiser, Jan Ferner, Stephan Philipp, Sridhar Sreeramulu, Betül Ceylan, Elke Stirnal, Alexandria Smart, Julian Schoth, Daniel Scheppa
article en
8 citations

Abstract

Targeting the RNA genome of SARS-CoV-2 is a viable option for antiviral drug development. We explored three ligand binding sites of the core pseudoknot RNA of the SARS-CoV-2 frameshift element. We iteratively optimized ligands, based on improved affinities, targeting these binding sites and report on structural and dynamic properties of the three identified binding sites. Available experimental 3D structures of the pseudoknot element were compared to SAXS and NMR data to validate its dominant folding state in solution. In order to experimentally map in silico predicted binding sites, NMR assignments of the majority of nucleobases were achieved by segmental labeling of the pseudoknot RNA and isotope-filtered NMR experiments at 1.2 GHz, demonstrating the value of NMR spectroscopy to supplement modelling and docking data. Optimized ligands with enhanced affinity were shown to specifically inhibit frameshifting without affecting 0-frame translation in cell-free translation assays, establishing the frameshift element as target for drug-like ligands of low molecular weight.

Angewandte Chemie International EditionVol. 64(9)
Goethe University Frankfurt (DE), OTH Regensburg (DE), Philipps University of Marburg (DE), Universitätsmedizin Greifswald (DE), Frankfurt Institute for Advanced Studies (DE), Universität Greifswald (DE), Helmholtz Centre for Infection Research (DE), Helmholtz Institute for RNA-based Infection Research (DE), University of Regensburg (DE)
Deutsche Forschungsgemeinschaft, Volkswagen Foundation, Deutsches Elektronen-Synchrotron, European Regional Development Fund
Good health and well-being
Openalex Percentile: Top 3%
RNA and protein synthesis mechanisms
6.45
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