Virus−Ligand Interactions: Identification and Characterization of Ligand Binding by NMR Spectroscopy
- 28 November 2002
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 125 (1) , 14-15
- https://doi.org/10.1021/ja027691e
Abstract
We demonstrate the detection and characterization of ligand binding to viruses via NMR. To illustrate the methodology, the interaction of an antiviral compound with human rhinovirus serotype 2 (HRV2) was investigated. Specific interaction of a capsid-binding inhibitor and native HRV2 was monitored utilizing saturation transfer difference (STD) NMR. STD NMR experiments at atomic resolution allowed those regions of the ligand that are involved in the interaction with the virus to be determined. The approach allows for (i) the fast and robust assessment of binding, (ii) the determination of the ligand binding epitope at atomic resolution without the necessity to crystallize virus−ligand complexes, and (iii) the reuse of the virus in subsequent assays. This methodology enables one to easily identify binding of drugs, peptides, and receptor or antibody fragments to the viral capsid.Keywords
This publication has 15 references indexed in Scilit:
- NMR-Based Screening with Competition Water−Ligand Observed via Gradient Spectroscopy Experiments: Detection of High-Affinity LigandsJournal of Medicinal Chemistry, 2002
- Complete Relaxation and Conformational Exchange Matrix (CORCEMA) Analysis of Intermolecular Saturation Transfer Effects in Reversibly Forming Ligand–Receptor ComplexesJournal of Magnetic Resonance, 2002
- Application of NMR Based Binding Assays to Identify Key Hydroxy Groups for Intermolecular RecognitionJournal of the American Chemical Society, 2000
- Characterization of Ligand Binding by Saturation Transfer Difference NMR SpectroscopyAngewandte Chemie International Edition in English, 1999
- Structural Studies on Human Rhinovirus 14 Drug-resistant Compensation MutantsJournal of Molecular Biology, 1995
- Proton nuclear magnetic resonance studies of the binding of sialosides to intact influenza virusVirology, 1992
- Structural analysis of a series of antiviral agents complexed with human rhinovirus 14.Proceedings of the National Academy of Sciences, 1988
- Nuclear magnetic resonance studies of the binding of trimethoprim to dihydrofolate reductaseBiochemistry, 1979
- Assignment of the heme c resonances in the 360 MHz 1H NMR spectra of cytochrome cBiochimica et Biophysica Acta (BBA) - Protein Structure, 1978
- Naturally occurring and artificially produced components of three rhinovirusesVirology, 1972