Literature DB >> 18216071

Observation of multiple folding pathways of beta-hairpin trpzip2 from independent continuous folding trajectories.

Changjun Chen1, Yi Xiao.   

Abstract

MOTIVATION: After 10-year investigations, the folding mechanisms of beta-hairpins are still under debate. Experiments strongly support zip-out pathway, while most simulations prefer the hydrophobic collapse model (including middle-out and zip-in pathways). In this article, we show that all pathways can occur during the folding of beta-hairpins but with different probabilities. The zip-out pathway is the most probable one. This is in agreement with the experimental results. We came to our conclusions by 38 100-ns room-temperature all-atom molecular dynamics simulations of the beta-hairpin trpzip2. Our results may help to clarify the inconsistencies in the current pictures of beta-hairpin folding mechanisms.

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Year:  2008        PMID: 18216071     DOI: 10.1093/bioinformatics/btn029

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  4 in total

1.  Enhanced sampling and applications in protein folding in explicit solvent.

Authors:  Cheng Zhang; Jianpeng Ma
Journal:  J Chem Phys       Date:  2010-06-28       Impact factor: 3.488

2.  Transient β-hairpin formation in α-synuclein monomer revealed by coarse-grained molecular dynamics simulation.

Authors:  Hang Yu; Wei Han; Wen Ma; Klaus Schulten
Journal:  J Chem Phys       Date:  2015-12-28       Impact factor: 3.488

3.  Correct folding of an α-helix and a β-hairpin using a polarized 2D torsional potential.

Authors:  Ya Gao; Yongxiu Li; Lirong Mou; Bingbing Lin; John Z H Zhang; Ye Mei
Journal:  Sci Rep       Date:  2015-06-03       Impact factor: 4.379

Review 4.  Folding mechanism of β-hairpin trpzip2: heterogeneity, transition state and folding pathways.

Authors:  Yi Xiao; Changjun Chen; Yi He
Journal:  Int J Mol Sci       Date:  2009-06-22       Impact factor: 6.208

  4 in total

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