Literature DB >> 10359778

Intermediates can accelerate protein folding.

C Wagner1, T Kiefhaber.   

Abstract

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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Year:  1999        PMID: 10359778      PMCID: PMC21981          DOI: 10.1073/pnas.96.12.6716

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  14 in total

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Journal:  Annu Rev Biochem       Date:  1990       Impact factor: 23.643

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Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

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Journal:  Science       Date:  1995-07-14       Impact factor: 47.728

Review 7.  Navigating the folding routes.

Authors:  P G Wolynes; J N Onuchic; D Thirumalai
Journal:  Science       Date:  1995-03-17       Impact factor: 47.728

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Authors:  W F Walkenhorst; S M Green; H Roder
Journal:  Biochemistry       Date:  1997-05-13       Impact factor: 3.162

10.  Temperature dependence of the hydrophobic interaction in protein folding.

Authors:  R L Baldwin
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

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  25 in total

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7.  Protein folding in high-dimensional spaces: hypergutters and the role of nonnative interactions.

Authors:  T C B McLeish
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8.  Role of unfolded state heterogeneity and en-route ruggedness in protein folding kinetics.

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10.  Exploring subdomain cooperativity in T4 lysozyme II: uncovering the C-terminal subdomain as a hidden intermediate in the kinetic folding pathway.

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