针对罕见事件动力学的路径采样与增强采样相结合

Dhiman, Ray
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引用次数: 0

摘要

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。
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Integrating Path Sampling with Enhanced Sampling for Rare-event Kinetics
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.
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