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Science 13 December 1991: Vol. 254. no. 5038, pp. 1598 - 1603 DOI: 10.1126/science.1749933
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Articles
Science, Vol 254, Issue 5038, 1598-1603
Copyright © 1991 by American Association for the Advancement of Science
The energy landscapes and motions of proteins
H Frauenfelder,
SG Sligar,
and
PG Wolynes
Center for Advanced Study, University of Illinois, Champaign, Urbana 61801.
Recent experiments, advances in theory, and analogies to other complex systems such as glasses and spin glasses yield insight into protein dynamics. The basis of the understanding is the observation that the energy landscape is complex: Proteins can assume a large number of nearly isoenergetic conformations (conformational substates). The concepts that emerge from studies of the conformational substates and the motions between them permit a quantitative discussion of one simple reaction, the binding of small ligands such as carbon monoxide to myoglobin.
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- On the nature of a glassy state of matter in a hydrated protein: Relation to protein function.
- M. M. Teeter, A. Yamano, B. Stec, and U. Mohanty (2001)
PNAS
98, 11242-11247
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- Inverse, protean, and ligand-selective agonism: matters of receptor conformation.
- T. KENAKIN (2001)
FASEB J
15, 598-611
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- Solvent dependence of dynamic transitions in protein solutions.
- V. Reat, R. Dunn, M. Ferrand, J. L. Finney, R. M. Daniel, and J. C. Smith (2000)
PNAS
97, 9961-9966
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