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How experiments see fluctuations of native proteins: Perspective from an exact model
Author(s) -
Tang Karen E. S.,
Dill Ken A.
Publication year - 1999
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/(sici)1097-461x(1999)75:3<147::aid-qua5>3.0.co;2-p
Subject(s) - native state , energy landscape , statistical physics , protein folding , folding (dsp implementation) , noise (video) , nuclear overhauser effect , physics , contrast (vision) , population , perspective (graphical) , protein structure , chemistry , nuclear magnetic resonance , biological system , nuclear magnetic resonance spectroscopy , biology , computer science , optics , artificial intelligence , thermodynamics , demography , sociology , electrical engineering , image (mathematics) , engineering
Proteins undergo fluctuations under native conditions. Many lines of evidence are usually interpreted as implying that fluctuations are small excursions away from the native structure. By definition, fluctuations from the native conformation are small increases in free energy. But if protein folding energy landscapes are bumpy, such fluctuations could involve highly nonnative but compact “misfolded” structures, even while the excursions in energy are small. Using a model in which we can rigorously study fluctuations and rugged energy landscapes, we ask whether current experimental measures of structure, such as X‐ray crystallographic Patterson maps and Debye–Waller factors or nuclear magnetic resonance (NMR) nuclear Overhauser effect (NOE) spectra, could detect bumpy landscapes. We find that even a substantial population of highly nonnative transients will generally be masked by the heavy averaging implicit in current experiments. This means that, in contrast to current interpretations, very nonnative or Misfold Fluctuations of native proteins may exist but are escaping experimental detection. A positive implication is that structure determination is robust to the presence of much conformational noise. ©1999 John Wiley & Sons, Inc. Int J Quant Chem 75: 147–164, 1999