Graduate School of Frontier Sciences, The University of Tokyo, Tokyo 113-0032, Japan.
J Chem Phys. 2010 Nov 14;133(18):185102. doi: 10.1063/1.3498745.
Protein dynamics evolves in a high-dimensional space, comprising aharmonic, strongly correlated motional modes. Such correlation often plays an important role in analyzing protein function. In order to identify significantly correlated collective motions, here we employ independent subspace analysis based on the subspace joint approximate diagonalization of eigenmatrices algorithm for the analysis of molecular dynamics (MD) simulation trajectories. From the 100 ns MD simulation of T4 lysozyme, we extract several independent subspaces in each of which collective modes are significantly correlated, and identify the other modes as independent. This method successfully detects the modes along which long-tailed non-Gaussian probability distributions are obtained. Based on the time cross-correlation analysis, we identified a series of events among domain motions and more localized motions in the protein, indicating the connection between the functionally relevant phenomena which have been independently revealed by experiments.
蛋白质动力学在一个高维空间中演变,包含一个调和的、强相关的运动模式。这种相关性在分析蛋白质功能时经常起着重要的作用。为了识别显著相关的集体运动,我们在这里采用基于子空间联合近似对角化本征矩阵算法的独立子空间分析来分析分子动力学(MD)模拟轨迹。从 T4 溶菌酶的 100ns MD 模拟中,我们在每个子空间中提取了几个显著相关的集体模式,并将其他模式识别为独立的。该方法成功地检测到了长尾非高斯概率分布所沿的模式。基于时间互相关分析,我们在蛋白质的结构域运动和更局部化的运动之间确定了一系列事件,表明了功能相关现象之间的联系,这些现象已经通过实验独立地揭示出来。