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Long-range electrostatic corrections in multipolar/polarizable QM/MM simulations.多极/可极化量子力学/分子力学模拟中的长程静电校正
Theor Chem Acc. 2016 Jul;135(7). doi: 10.1007/s00214-016-1923-8. Epub 2016 Jun 17.
2
Efficient Atomistic Simulation of Pathways and Calculation of Rate Constants for a Protein-Peptide Binding Process: Application to the MDM2 Protein and an Intrinsically Disordered p53 Peptide.蛋白质-肽结合过程的途径高效原子模拟及速率常数计算:应用于MDM2蛋白和一种内在无序的p53肽
J Phys Chem Lett. 2016 Sep 1;7(17):3440-5. doi: 10.1021/acs.jpclett.6b01502. Epub 2016 Aug 22.
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Accurate Estimation of Protein Folding and Unfolding Times: Beyond Markov State Models.蛋白质折叠与解折叠时间的准确估计:超越马尔可夫状态模型
J Chem Theory Comput. 2016 Aug 9;12(8):3473-81. doi: 10.1021/acs.jctc.6b00339. Epub 2016 Jul 11.
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Ligand Release Pathways Obtained with WExplore: Residence Times and Mechanisms.通过WExplore获得的配体释放途径:停留时间和机制
J Phys Chem B. 2016 Jun 23;120(24):5377-85. doi: 10.1021/acs.jpcb.6b04012. Epub 2016 Jun 8.
5
Unbiased Rare Event Sampling in Spatial Stochastic Systems Biology Models Using a Weighted Ensemble of Trajectories.基于轨迹加权系综的空间随机系统生物学模型中的无偏稀有事件采样
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6
Tabulation as a high-resolution alternative to coarse-graining protein interactions: Initial application to virus capsid subunits.作为粗粒化蛋白质相互作用的高分辨率替代方法的表格化:对病毒衣壳亚基的初步应用。
J Chem Phys. 2015 Dec 28;143(24):243159. doi: 10.1063/1.4938479.
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Highly Efficient Computation of the Basal kon using Direct Simulation of Protein-Protein Association with Flexible Molecular Models.使用灵活分子模型对蛋白质-蛋白质缔合进行直接模拟来高效计算基础kon值。
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GROMACS 4:  Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation.GROMACS 4:高效、负载均衡和可扩展的分子模拟算法。
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Striking Effects of Hydrodynamic Interactions on the Simulated Diffusion and Folding of Proteins.流体动力学相互作用对蛋白质模拟扩散和折叠的显著影响。
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加权集成模拟:方法、应用及软件综述

Weighted Ensemble Simulation: Review of Methodology, Applications, and Software.

作者信息

Zuckerman Daniel M, Chong Lillian T

机构信息

Department of Biomedical Engineering, Oregon Health and Science University, Portland, Oregon 97239; email:

Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260; email:

出版信息

Annu Rev Biophys. 2017 May 22;46:43-57. doi: 10.1146/annurev-biophys-070816-033834. Epub 2017 Mar 1.

DOI:10.1146/annurev-biophys-070816-033834
PMID:28301772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5896317/
Abstract

The weighted ensemble (WE) methodology orchestrates quasi-independent parallel simulations run with intermittent communication that can enhance sampling of rare events such as protein conformational changes, folding, and binding. The WE strategy can achieve superlinear scaling-the unbiased estimation of key observables such as rate constants and equilibrium state populations to greater precision than would be possible with ordinary parallel simulation. WE software can be used to control any dynamics engine, such as standard molecular dynamics and cell-modeling packages. This article reviews the theoretical basis of WE and goes on to describe successful applications to a number of complex biological processes-protein conformational transitions, (un)binding, and assembly processes, as well as cell-scale processes in systems biology. We furthermore discuss the challenges that need to be overcome in the next phase of WE methodological development. Overall, the combined advances in WE methodology and software have enabled the simulation of long-timescale processes that would otherwise not be practical on typical computing resources using standard simulation.

摘要

加权系综(WE)方法协调了通过间歇性通信运行的准独立并行模拟,这可以增强对罕见事件(如蛋白质构象变化、折叠和结合)的采样。WE策略可以实现超线性缩放——对关键可观测量(如速率常数和平衡态种群)进行无偏估计,其精度比普通并行模拟更高。WE软件可用于控制任何动力学引擎,如标准分子动力学和细胞建模软件包。本文回顾了WE的理论基础,并继续描述了其在许多复杂生物过程中的成功应用——蛋白质构象转变、(非)结合和组装过程,以及系统生物学中的细胞尺度过程。我们还讨论了WE方法学下一阶段发展中需要克服的挑战。总体而言,WE方法和软件的综合进步使得模拟长时间尺度过程成为可能,否则使用标准模拟在典型计算资源上是不切实际的。