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过渡温度元动力学是研究类药物分子透过膜渗透的一种有前途的工具。

Transition-Tempered Metadynamics Is a Promising Tool for Studying the Permeation of Drug-like Molecules through Membranes.

作者信息

Sun Rui, Dama James F, Tan Jeffrey S, Rose John P, Voth Gregory A

机构信息

Department of Chemistry, Institute for Biophysical Dynamics, James Franck Institute, and Computation Institute, The University of Chicago , 5735 South Ellis Avenue, Chicago, Illinois 60637, United States.

Small Molecule Design & Development, Lilly Corporate Center, Eli Lilly & Company, Indianapolis, Indiana 46285, United States.

出版信息

J Chem Theory Comput. 2016 Oct 11;12(10):5157-5169. doi: 10.1021/acs.jctc.6b00206. Epub 2016 Sep 22.

Abstract

Metadynamics is an important enhanced sampling technique in molecular dynamics simulation to efficiently explore potential energy surfaces. The recently developed transition-tempered metadynamics (TTMetaD) has been proven to converge asymptotically without sacrificing exploration of the collective variable space in the early stages of simulations, unlike other convergent metadynamics (MetaD) methods. We have applied TTMetaD to study the permeation of drug-like molecules through a lipid bilayer to further investigate the usefulness of this method as applied to problems of relevance to medicinal chemistry. First, ethanol permeation through a lipid bilayer was studied to compare TTMetaD with nontempered metadynamics and well-tempered metadynamics. The bias energies computed from various metadynamics simulations were compared to the potential of mean force calculated from umbrella sampling. Though all of the MetaD simulations agree with one another asymptotically, TTMetaD is able to predict the most accurate and reliable estimate of the potential of mean force for permeation in the early stages of the simulations and is robust to the choice of required additional parameters. We also show that using multiple randomly initialized replicas allows convergence analysis and also provides an efficient means to converge the simulations in shorter wall times and, more unexpectedly, in shorter CPU times; splitting the CPU time between multiple replicas appears to lead to less overall error. After validating the method, we studied the permeation of a more complicated drug-like molecule, trimethoprim. Three sets of TTMetaD simulations with different choices of collective variables were carried out, and all converged within feasible simulation time. The minimum free energy paths showed that TTMetaD was able to predict almost identical permeation mechanisms in each case despite significantly different definitions of collective variables.

摘要

元动力学是分子动力学模拟中一种重要的增强采样技术,用于有效探索势能面。最近开发的过渡温度元动力学(TTMetaD)已被证明能渐近收敛,且在模拟早期不会牺牲对集体变量空间的探索,这与其他收敛性元动力学(MetaD)方法不同。我们应用TTMetaD来研究类药物分子通过脂质双层的渗透,以进一步探究该方法在与药物化学相关问题上的实用性。首先,研究了乙醇通过脂质双层的渗透,将TTMetaD与非温度元动力学和良好温度元动力学进行比较。将各种元动力学模拟计算得到的偏差能量与伞形采样计算得到的平均力势进行比较。尽管所有的MetaD模拟在渐近情况下相互一致,但TTMetaD能够在模拟早期预测出最准确、最可靠的渗透平均力势估计值,并且对所需附加参数的选择具有鲁棒性。我们还表明,使用多个随机初始化的副本可以进行收敛性分析,并且还提供了一种在更短的实际运行时间内收敛模拟的有效方法,更出乎意料的是,在更短的CPU时间内也能收敛;将CPU时间分配到多个副本之间似乎会导致总体误差更小。在验证该方法后,我们研究了一种更复杂的类药物分子甲氧苄啶的渗透。进行了三组具有不同集体变量选择的TTMetaD模拟,并且所有模拟都在可行的模拟时间内收敛。最小自由能路径表明,尽管集体变量的定义有显著差异,但TTMetaD在每种情况下都能够预测几乎相同的渗透机制。

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