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使用基于强化学习的加权集成方法进行稀有事件采样。

Rare-Event Sampling using a Reinforcement Learning-Based Weighted Ensemble Method.

作者信息

Yang Darian T, Goldberg Alex M, Chong Lillian T

机构信息

Molecular Biophysics and Structural Biology Graduate Program, University of Pittsburgh and Carnegie Mellon University, Pittsburgh, Pennsylvania 15260.

Department of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15260.

出版信息

bioRxiv. 2024 Oct 11:2024.10.09.617475. doi: 10.1101/2024.10.09.617475.

DOI:10.1101/2024.10.09.617475
PMID:39416089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11482931/
Abstract

Despite the power of path sampling strategies in enabling simulations of rare events, such strategies have not reached their full potential. A common challenge that remains is the identification of a progress coordinate that captures the slow relevant motions of a rare event. Here we have developed a weighted ensemble (WE) path sampling strategy that exploits reinforcement learning to automatically identify an effective progress coordinate among a set of potential coordinates during a simulation. We apply our WE strategy with reinforcement learning to three benchmark systems: (i) an egg carton-shaped toy potential, (ii) an S-shaped toy potential, and (iii) a dimer of the HIV-1 capsid protein (C-terminal domain). To enable rapid testing of the latter system at the atomic level, we employed discrete-state synthetic molecular dynamics trajectories using a generative, fine-grained Markov state model that was based on extensive conventional simulations. Our results demonstrate that using concepts from reinforcement learning with a weighted ensemble of trajectories automatically identifies relevant progress co-ordinates among multiple candidates at a given time during a simulation. Due to the rigorous weighting of trajectories, the simulations maintain rigorous kinetics.

摘要

尽管路径采样策略在实现罕见事件模拟方面具有强大功能,但这些策略尚未充分发挥其潜力。仍然存在的一个常见挑战是确定一个能够捕捉罕见事件缓慢相关运动的进展坐标。在此,我们开发了一种加权系综(WE)路径采样策略,该策略利用强化学习在模拟过程中从一组潜在坐标中自动识别出有效的进展坐标。我们将带有强化学习的WE策略应用于三个基准系统:(i)一个蛋盒形状的玩具势;(ii)一个S形玩具势;以及(iii)HIV-1衣壳蛋白(C末端结构域)的二聚体。为了能够在原子水平上快速测试后一个系统,我们使用了基于广泛传统模拟的生成式、细粒度马尔可夫状态模型的离散状态合成分子动力学轨迹。我们的结果表明,将强化学习的概念与轨迹的加权系综相结合,能够在模拟过程中的给定时间自动从多个候选坐标中识别出相关的进展坐标。由于对轨迹进行了严格加权,模拟保持了严格的动力学。

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本文引用的文献

1
Unsupervised Learning of Progress Coordinates during Weighted Ensemble Simulations: Application to NTL9 Protein Folding.加权系综模拟中进展坐标的无监督学习:应用于NTL9蛋白质折叠
J Chem Theory Comput. 2025 Apr 8;21(7):3691-3699. doi: 10.1021/acs.jctc.4c01136. Epub 2025 Mar 19.
2
WEDAP: A Python Package for Streamlined Plotting of Molecular Simulation Data.WEDAP:用于简化分子模拟数据绘图的 Python 包。
J Chem Inf Model. 2024 Aug 12;64(15):5749-5755. doi: 10.1021/acs.jcim.4c00867. Epub 2024 Jul 16.
3
Enhanced Sampling with Machine Learning.
利用机器学习的增强采样
Annu Rev Phys Chem. 2024 Jun;75(1):347-370. doi: 10.1146/annurev-physchem-083122-125941. Epub 2024 Jun 14.
4
Collective Variable-Based Enhanced Sampling: From Human Learning to Machine Learning.基于整体变量的增强采样:从人类学习到机器学习。
J Phys Chem Lett. 2024 Feb 15;15(6):1774-1783. doi: 10.1021/acs.jpclett.3c03542. Epub 2024 Feb 8.
5
Adaptive Sampling Methods for Molecular Dynamics in the Era of Machine Learning.机器学习时代的分子动力学自适应采样方法。
J Phys Chem B. 2023 Dec 21;127(50):10669-10681. doi: 10.1021/acs.jpcb.3c04843. Epub 2023 Dec 11.
6
Building insightful, memory-enriched models to capture long-time biochemical processes from short-time simulations.从短时间模拟中构建有洞察力、丰富记忆的模型,以捕捉长时间的生化过程。
Proc Natl Acad Sci U S A. 2023 Mar 21;120(12):e2221048120. doi: 10.1073/pnas.2221048120. Epub 2023 Mar 15.
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LAST: Latent Space-Assisted Adaptive Sampling for Protein Trajectories.LAST:用于蛋白质轨迹的潜在空间辅助自适应采样。
J Chem Inf Model. 2023 Jan 9;63(1):67-75. doi: 10.1021/acs.jcim.2c01213. Epub 2022 Dec 6.
8
WESTPA 2.0: High-Performance Upgrades for Weighted Ensemble Simulations and Analysis of Longer-Timescale Applications.WESTPA 2.0:加权集成模拟的高性能升级以及更长时间尺度应用的分析。
J Chem Theory Comput. 2022 Feb 8;18(2):638-649. doi: 10.1021/acs.jctc.1c01154. Epub 2022 Jan 19.
9
What Markov State Models Can and Cannot Do: Correlation versus Path-Based Observables in Protein-Folding Models.马尔可夫状态模型能做什么与不能做什么:蛋白质折叠模型中基于相关性与基于路径的可观测量
J Chem Theory Comput. 2021 May 11;17(5):3119-3133. doi: 10.1021/acs.jctc.0c01154. Epub 2021 Apr 27.
10
On the advantages of exploiting memory in Markov state models for biomolecular dynamics.利用马尔可夫状态模型中的记忆来研究生物分子动力学的优势。
J Chem Phys. 2020 Jul 7;153(1):014105. doi: 10.1063/5.0010787.