Intermediates can Accelerate Protein Folding

The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers crea...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1999-06, Vol.96 (12), p.6716-6721
Hauptverfasser: Wagner, Clemens, Kiephaber, Thomas
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Kiephaber, Thomas
description The effect of intermediates on the rate of protein folding is explored by applying Kramers' theory of diffusive barrier crossing in the high friction limit. Intermediates are represented as local minima in the transition barrier. We observe that very large or very small additional barriers created by the intermediates slow down the folding process. The rate of folding markedly increases, however, when the additional barriers become >1 kBT but leave the overall barrier height unchanged. This rate-enhancing effect is caused by a favorable entropic contribution to the free energy of activation, and it increases with the number of intermediates up to a limiting value. From these calculations, we conclude that optimized transition barriers should contain partially folded high energy intermediates.
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source Jstor Complete Legacy; MEDLINE; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Animals
Biological Sciences
Coordinate systems
Curvature
Eigenvalues
Energy
Energy levels
Entropy
Experiments
Humans
Kinetics
Local minimum
Models, Chemical
Molecules
Protein Folding
Proteins
Proteins - chemistry
Theory
title Intermediates can Accelerate Protein Folding
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