Pujan Ajmera, Santiago Vargas, Shobhit S Chaturvedi, Matthew Hennefarth, Anastassia N Alexandrova
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引用次数: 0
摘要
静电预组织是了解酶的催化功能的一种令人兴奋的模式,但现有的计算分析工具有限。特别是,没有方法可以解释蛋白质活性位点中三维电场E - l (r)的几何、动力学和基本组成部分。为了解决这个问题,我们提出了PyCPET (Python Computation of Electric Field topology),这是一个全面的开源工具箱,用于分析酶中的E - l (r)。我们设计它围绕计算效率和用户友好与CPU和gpu加速代码。我们的目标是为酶系统的丰富、描述性分析提供一组功能,包括动力学、基准测试、3D E - l (r)中的流线分布分析、点E - l (r)的计算、主成分分析和3D E - l (r)可视化。最后,我们通过探索三种情况下静电预组织和动力学的性质来证明其多功能性:细胞色素C,共取代肝醇脱氢酶和HIV蛋白酶。这些测试系统,连同之前的工作,建立了PyCPET作为深入分析和可视化酶电场的基本工具包,为理解静电对酶催化的贡献开辟了新的途径。
PyCPET─Computing Heterogeneous 3D Protein Electric Fields and Their Dynamics.
Electrostatic preorganization is an exciting mode to understand the catalytic function of enzymes, yet limited tools exist to computationally analyze it. In particular, no methods exist to interpret the geometry, dynamics, and fundamental components of 3D electric fields, E⃗(r), in protein active sites. To address this, we present PyCPET (Python Computation of Electric Field Topologies), a comprehensive, open-source toolbox to analyze E⃗(r) in enzymes. We designed it around computational efficiency and user friendliness with both CPU- and GPU-accelerated codes. Our aim is to provide a set of functions for rich, descriptive analysis of enzyme systems including dynamics, benchmarking, distribution of streamlines analysis in 3D E⃗(r), computation of point E⃗(r), principal component analysis, and 3D E⃗(r) visualization. Finally, we demonstrate its versatility by exploring the nature of electrostatic preorganization and dynamics in three cases: Cytochrome C, Co-substituted Liver Alcohol Dehydrogenase, and HIV Protease. These test systems, along with previous work, establish PyCPET as an essential toolkit for the in-depth analysis and visualization of electric fields in enzymes, unlocking new avenues for understanding electrostatic contributions to enzyme catalysis.
期刊介绍:
The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.