Two-dimensional infrared spectra reveal relaxation of the nonnucleoside inhibitor TMC278 complexed with HIV-1 reverse transcriptase
- 5 February 2008
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 105 (5) , 1472-1477
- https://doi.org/10.1073/pnas.0709320104
Abstract
The two nitrile groups at the wings of the nonnucleoside HIV-1 reverse transcriptase (RT) inhibitor TMC278 are both identified in high-sensitivity 2D IR spectroscopy experiments of the HIV-1 RT/TMC278 complex. The vibrational spectra indicate that the two arms of the inhibitor sense quite different environments within the hydrophobic pocket. The vibrational relaxation of the two arms are almost equal at 3 ps from model studies. The 2D IR spectra expose a significant distribution of nitrile frequencies that diffuse at equilibrium on ultrafast time scales ranging from hundreds of femtoseconds to tens of picoseconds. The slow spectral diffusion of the cyanovinyl arm of the inhibitor is attributed to its interaction with the backbone and side chains in the hydrophobic tunnel. The results show that the inhibitor cyano modes lose memory of their structural configurations relative to the hydrophobic pocket within tens of picoseconds. The cross-peaks between the two arms of the drug are tentatively attributed to relaxation of the nitrile state with both arms excited.Keywords
This publication has 63 references indexed in Scilit:
- Improved identification of metabolites in complex mixtures using HSQC NMR spectroscopyAnalytica Chimica Acta, 2008
- Method for Determining Molar Concentrations of Metabolites in Complex Solutions from Two-Dimensional 1H−13C NMR SpectraAnalytical Chemistry, 2007
- A relaxation-assisted 2D IR spectroscopy methodProceedings of the National Academy of Sciences, 2007
- Hydrogen Bond Lifetimes and Energetics for Solute/Solvent Complexes Studied with 2D-IR Vibrational Echo SpectroscopyJournal of the American Chemical Society, 2007
- Substrate binding and protein conformational dynamics measured by 2D-IR vibrational echo spectroscopyProceedings of the National Academy of Sciences, 2007
- Two-dimensional vibrational optical probes for peptide fast folding investigationProceedings of the National Academy of Sciences, 2006
- Amide vibrations are delocalized across the hydrophobic interface of a transmembrane helix dimerProceedings of the National Academy of Sciences, 2006
- Targeted Profiling: Quantitative Analysis of 1H NMR Metabolomics DataAnalytical Chemistry, 2006
- NMRPipe: A multidimensional spectral processing system based on UNIX pipesJournal of Biomolecular NMR, 1995
- A relational database for sequence-specific protein NMR dataJournal of Biomolecular NMR, 1991