Integrating Path Sampling with Enhanced Sampling for Rare-event Kinetics

Dhiman, Ray
{"title":"Integrating Path Sampling with Enhanced Sampling for Rare-event Kinetics","authors":"Dhiman, Ray","doi":"10.26434/chemrxiv-2024-qr6kv","DOIUrl":null,"url":null,"abstract":"Studying the kinetics of long-timescale rare events is a fundamental challenge in molecular simulation. To address this problem, we propose an integration of two different rare-event sampling philosophies: biased enhanced sampling and unbiased path sampling. Enhanced sampling methods e.g. metadynamics can facilitate enthalpic barrier crossing by applying an external bias potential. On the contrary, path sampling methods like weighted ensemble (WE) lack explicit mechanisms to overcome energetic barriers. However, they can accelerate the exploration of rugged free energy surfaces through trajectory resampling. We show that a judicious combination of the weighted ensemble with a metadynamics-like algorithm, can synergize the strengths and mitigate the deficiencies of path sampling and enhanced sampling approaches. The resulting integrated sampling (IS) algorithm improves the computational efficiency of calculating the kinetics of peptide conformational transitions, protein unfolding, and the dissociation of a ligand-receptor complex. Furthermore, the IS approach can direct sampling along the minimum free energy pathway even when the collective variable used for biasing is suboptimal. These advantages make the integrated sampling algorithm suitable for studying the kinetics of complex molecular systems of biological and pharmaceutical relevance.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-qr6kv","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Studying the kinetics of long-timescale rare events is a fundamental challenge in molecular simulation. To address this problem, we propose an integration of two different rare-event sampling philosophies: biased enhanced sampling and unbiased path sampling. Enhanced sampling methods e.g. metadynamics can facilitate enthalpic barrier crossing by applying an external bias potential. On the contrary, path sampling methods like weighted ensemble (WE) lack explicit mechanisms to overcome energetic barriers. However, they can accelerate the exploration of rugged free energy surfaces through trajectory resampling. We show that a judicious combination of the weighted ensemble with a metadynamics-like algorithm, can synergize the strengths and mitigate the deficiencies of path sampling and enhanced sampling approaches. The resulting integrated sampling (IS) algorithm improves the computational efficiency of calculating the kinetics of peptide conformational transitions, protein unfolding, and the dissociation of a ligand-receptor complex. Furthermore, the IS approach can direct sampling along the minimum free energy pathway even when the collective variable used for biasing is suboptimal. These advantages make the integrated sampling algorithm suitable for studying the kinetics of complex molecular systems of biological and pharmaceutical relevance.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
针对罕见事件动力学的路径采样与增强采样相结合
研究长时间尺度罕见事件的动力学是分子模拟的一项基本挑战。为解决这一问题,我们提出了两种不同稀有事件采样理念的整合方案:有偏增强采样和无偏路径采样。增强采样方法(如元动力学)可通过应用外部偏置电势促进焓障穿越。相反,加权集合(WE)等路径采样方法缺乏克服能量障碍的明确机制。不过,它们可以通过轨迹重采样加速探索崎岖的自由能表面。我们的研究表明,将加权集合与类似于元动力学的算法明智地结合起来,可以协同路径采样和增强采样方法的优势并减轻它们的不足。由此产生的集成采样(IS)算法提高了计算肽构象转变、蛋白质解折和配体-受体复合物解离动力学的计算效率。此外,即使用于偏置的集合变量不理想,IS 方法也能引导采样沿着最小自由能路径进行。这些优势使集成采样算法适用于研究与生物和制药相关的复杂分子系统的动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Exascale Quantum Mechanical Simulations: Navigating the Shifting Sands of Hardware and Software Hybrid synthesis of AMFC-derived amides using supported gold nanoparticles and acyl-coenzyme A ligases Non-covalent spin labelling of TRPC5 ion channels enables EPR studies of protein-ligand interactions An Efficient RI-MP2 Algorithm for Distributed Many-GPU Architectures Unusual Confinement-Induced Basicity and Proton-Mediated CH Activity of an Adipic Acid-Ammonium Cluster
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1