Efficient perturbation analysis of elastic network models - Application to acetylcholinesterase of T. californica

被引:1
作者
Hamacher, K. [1 ]
机构
[1] Tech Univ Darmstadt, Bioinformat & Theo Biol Grp, D-64287 Darmstadt, Germany
关键词
Elastic network models; Molecular biophysics; Sensitivity analysis; Molecular evolution; Linear algebra; MOLECULAR-DYNAMICS; VIBRATIONAL DYNAMICS; SINGLE-PARAMETER; FLUCTUATIONS; PROTEINS; OPTIMIZATION;
D O I
10.1016/j.jcp.2010.06.015
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Elastic network models in their different flavors have become useful models for the dynamics and functions of biomolecular systems such as proteins and their complexes. Perturbation to the interactions occur due to randomized and fixated changes (in molecular evolution) or designed modifications of the protein structures (in bioengineering). These perturbations are modifications in the topology and the strength of the interactions modeled by the elastic network models. We discuss how a naive approach to compute properties for a large number of perturbed structures and interactions by repeated diagonalization can be replaced with an identity found in linear algebra. We argue about the computational complexity and discuss the advantages of the protocol. We apply the proposed algorithm to the acetylcholinesterase, a well-known enzyme in neurobiology, and show how one can gain insight into the "breathing dynamics" of a structural funnel necessary for the function of the protein. The computational speed-up was a 60-fold increase in this example. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:7309 / 7316
页数:8
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