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Observation of multiple folding pathways of β-hairpin trpzip2 from independent continuous folding trajectories
Author(s) -
Changjun Chen,
Yi Xiao
Publication year - 2008
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btn029
Subject(s) - folding (dsp implementation) , protein folding , computer science , computational biology , downhill folding , biological system , algorithm , biophysics , chemistry , biology , biochemistry , phi value analysis , engineering , electrical engineering
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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