Replica Exchange with Guided Annealing for Accelerated Sampling of Disordered Protein Conformations

被引:13
作者
Zhang, Weihong [1 ]
Chen, Jianhan [1 ]
机构
[1] Kansas State Univ, Dept Biochem & Mol Biophys, Manhattan, KS 66506 USA
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
protein folding; enhanced sampling; molecular dynamics; intrinsically disordered proteins; structural ensemble; MOLECULAR-DYNAMICS SIMULATIONS; TRANSACTIVATION DOMAIN; NMR STRUCTURES; MODELS; ENERGY; EFFICIENCY; SOLVATION; CONVERGENCE; TRANSITIONS; EQUILIBRIA;
D O I
10.1002/jcc.23675
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We critically examine a recently proposed convective replica exchange (cRE) method for enhanced sampling of protein conformation based on theoretical and numerical analysis. The results demonstrate that cRE and related replica exchange with guided annealing (RE-GA) schemes lead to unbalanced exchange attempt probabilities and break detailed balance whenever the system undergoes slow conformational transitions (relative to the temperature diffusion timescale). Nonetheless, numerical simulations suggest that approximate canonical ensembles can be generated for systems with small conformational transition barriers. This suggests that RE-GA maybe suitable for simulating intrinsically disordered proteins, an important class of newly recognized functional proteins. The efficacy of RE-GA is demonstrated by calculating the conformational ensembles of intrinsically disordered kinase inducible domain protein. The results show that RE-GA helps the protein to escape nonspecific compact states more efficiently and provides several fold speedups in generating converged and largely correct ensembles compared to the standard temperature RE. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:1682 / 1689
页数:8
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