分子动力学模拟中可极化高斯多极模型的性能调整

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Zhen Huang, Yongxian Wu, Yong Duan* and Ray Luo*, 
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引用次数: 0

摘要

分子动力学(MD)模拟对于理解原子水平上的分子现象至关重要,其准确性很大程度上取决于所使用的力场和采样。包含原子极化效应的极化力场是模拟技术的重大进步。极化高斯多极(pGM)模型以其精确再现从头算静电相互作用而闻名。在本研究中,我们记录了我们在AMBER框架中使用MPI(消息传递接口)来提高pGM模拟的计算效率和可扩展性的努力。性能评估表明,我们基于mpi的pGM模型在保持计算精度的同时显著减少了运行时间和有效缩放。此外,我们还研究了在NVE仿真集成下MPI实现的稳定性和可靠性。探讨了pGM模型的最优Ewald参数和感应参数,并在各种模拟集成下评估了其统计特性。我们的研究结果表明,mpi实现在延长的仿真时间内保持了增强的稳定性和鲁棒性。我们进一步评估了模型在NVT(恒定数量、体积和温度)和NPT(恒定数量、压力和温度)组合下的性能,并评估了不同时间步长和收敛容差对诱导偶极子计算的影响。从这些练习中吸取的经验教训有望帮助用户在模拟设置方面做出明智的决策。这些集成下性能的提高使得研究更大的分子系统成为可能,从而扩大了pGM模型在详细MD模拟中的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Performance Tuning of Polarizable Gaussian Multipole Model in Molecular Dynamics Simulations

Performance Tuning of Polarizable Gaussian Multipole Model in Molecular Dynamics Simulations

Molecular dynamics (MD) simulations are essential for understanding molecular phenomena at the atomic level, with their accuracy largely dependent on both the employed force field and sampling. Polarizable force fields, which incorporate atomic polarization effects, represent a significant advancement in simulation technology. The polarizable Gaussian multipole (pGM) model has been noted for its accurate reproduction of ab initio electrostatic interactions. In this study, we document our effort to enhance the computational efficiency and scalability of the pGM simulations within the AMBER framework using MPI (message passing interface). Performance evaluations reveal that our MPI-based pGM model significantly reduces runtime and scales effectively while maintaining computational accuracy. Additionally, we investigated the stability and reliability of the MPI implementation under the NVE simulation ensemble. Optimal Ewald and induction parameters for the pGM model are also explored, and its statistical properties are assessed under various simulation ensembles. Our findings demonstrate that the MPI-implementation maintains enhanced stability and robustness during extended simulation times. We further evaluated the model performance under both NVT (constant number, volume, and temperature) and NPT (constant number, pressure, and temperature) ensembles and assessed the effects of varying timesteps and convergence tolerance on induced dipole calculations. The lessons learned from these exercises are expected to help the users to make informed decisions on simulation setup. The improved performance under these ensembles enables the study of larger molecular systems, thereby expanding the applicability of the pGM model in detailed MD simulations.

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来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
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.
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