Literature DB >> 17073456

A simple semiempirical model for the effect of molecular confinement upon the rate of protein folding.

Manajit Hayer-Hartl1, Allen P Minton.   

Abstract

A simple two-state model for the dependence of the rate of folding of a polypeptide confined within a spherical cavity upon the size of the cavity relative to that of the polypeptide is presented. A general prediction of the model is that decreasing the size of the cavity will increase the rate of refolding until the cavity becomes only slightly larger than the native state of the protein, at which point a further decrease in cavity size decreases the rate of refolding. The model qualitatively accounts for the behavior of several previously published simulations of folding within a cavity, as well as recently reported experimental measurements of the relative rate of refolding of each of five proteins encapsulated within wild-type and mutant GroEL-GroES complexes that have been engineered to provide internal cavities with similar surface composition and varying volume.

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Year:  2006        PMID: 17073456     DOI: 10.1021/bi061597j

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  24 in total

Review 1.  Protein folding in the cytoplasm and the heat shock response.

Authors:  R Martin Vabulas; Swasti Raychaudhuri; Manajit Hayer-Hartl; F Ulrich Hartl
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-12       Impact factor: 10.005

Review 2.  Protein folding in confined and crowded environments.

Authors:  Huan-Xiang Zhou
Journal:  Arch Biochem Biophys       Date:  2007-08-01       Impact factor: 4.013

Review 3.  Converging concepts of protein folding in vitro and in vivo.

Authors:  F Ulrich Hartl; Manajit Hayer-Hartl
Journal:  Nat Struct Mol Biol       Date:  2009-06       Impact factor: 15.369

4.  Thermodynamics and kinetics of protein folding under confinement.

Authors:  Jeetain Mittal; Robert B Best
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-10       Impact factor: 11.205

Review 5.  Development of free-energy-based models for chaperonin containing TCP-1 mediated folding of actin.

Authors:  Gabriel M Altschuler; Keith R Willison
Journal:  J R Soc Interface       Date:  2008-12-06       Impact factor: 4.118

6.  Effect of interactions with the chaperonin cavity on protein folding and misfolding.

Authors:  Anshul Sirur; Michael Knott; Robert B Best
Journal:  Phys Chem Chem Phys       Date:  2013-09-27       Impact factor: 3.676

7.  The effects of macromolecular crowding on the mechanical stability of protein molecules.

Authors:  Jian-Min Yuan; Chia-Lin Chyan; Huan-Xiang Zhou; Tse-Yu Chung; Haibo Peng; Guanghui Ping; Guoliang Yang
Journal:  Protein Sci       Date:  2008-09-09       Impact factor: 6.725

8.  Effect of mixed macromolecular crowding agents on protein folding.

Authors:  Huan-Xiang Zhou
Journal:  Proteins       Date:  2008-09

Review 9.  Macromolecular crowding and confinement: biochemical, biophysical, and potential physiological consequences.

Authors:  Huan-Xiang Zhou; Germán Rivas; Allen P Minton
Journal:  Annu Rev Biophys       Date:  2008       Impact factor: 12.981

10.  GroEL/ES chaperonin modulates the mechanism and accelerates the rate of TIM-barrel domain folding.

Authors:  Florian Georgescauld; Kristina Popova; Amit J Gupta; Andreas Bracher; John R Engen; Manajit Hayer-Hartl; F Ulrich Hartl
Journal:  Cell       Date:  2014-05-08       Impact factor: 41.582

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