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混合模拟:使用虚拟位点将原子和粗粒力场结合。

Hybrid simulations: combining atomistic and coarse-grained force fields using virtual sites.

机构信息

Groningen Biomolecular Sciences and Biotechnology Institute & Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 7, 9747 AG Groningen, The Netherlands.

出版信息

Phys Chem Chem Phys. 2011 Jun 14;13(22):10437-48. doi: 10.1039/c0cp02981e. Epub 2011 Apr 15.

Abstract

Hybrid simulations, in which part of the system is represented at atomic resolution and the remaining part at a reduced, coarse-grained, level offer a powerful way to combine the accuracy associated with the atomistic force fields to the sampling speed obtained with coarse-grained (CG) potentials. In this work we introduce a straightforward scheme to perform hybrid simulations, making use of virtual sites to couple the two levels of resolution. With the help of these virtual sites interactions between molecules at different levels of resolution, i.e. between CG and atomistic molecules, are treated the same way as the pure CG-CG interactions. To test our method, we combine the Gromos atomistic force field with a number of coarse-grained potentials, obtained through several approaches that are designed to obtain CG potentials based on an existing atomistic model, namely iterative Boltzmann inversion, force matching, and a potential of mean force subtraction procedure (SB). We also explore the use of the MARTINI force field for the CG potential. A simple system, consisting of atomistic butane molecules dissolved in CG butane, is used to study the performance of our hybrid scheme. Based on the potentials of mean force for atomistic butane in CG solvent, and the properties of 1:1 mixtures of atomistic and CG butane which should exhibit ideal mixing behavior, we conclude that the MARTINI and SB potentials are particularly suited to be combined with the atomistic force field. The MARTINI potential is subsequently used to perform hybrid simulations of atomistic dialanine peptides in both CG butane and water. Compared to a fully atomistic description of the system, the hybrid description gives similar results provided that the dielectric screening of water is accounted for. Within the field of biomolecules, our method appears ideally suited to study e.g. protein-ligand binding, where the active site and ligand are modeled in atomistic detail and the rest of the protein, together with the solvent, is coarse-grained.

摘要

混合模拟,其中系统的一部分以原子分辨率表示,其余部分以简化的粗粒度表示,提供了一种将与原子力场相关的准确性与粗粒度(CG)势获得的采样速度相结合的强大方法。在这项工作中,我们引入了一种直接的混合模拟方案,利用虚拟站点将两个分辨率级别耦合在一起。借助这些虚拟站点,可以以与纯 CG-CG 相互作用相同的方式处理不同分辨率水平(即 CG 和原子分子之间)的分子之间的相互作用。为了测试我们的方法,我们将 Gromos 原子力场与一些粗粒度势结合在一起,这些粗粒度势是通过几种方法获得的,这些方法旨在基于现有的原子模型获得 CG 势,即迭代玻尔兹曼反演、力匹配和平均力势减法程序(SB)。我们还探索了使用 MARTINI 力场作为 CG 势。使用由原子但烷分子溶解在 CG 但烷中组成的简单系统来研究我们的混合方案的性能。基于 CG 溶剂中原子但烷的平均力势以及原子但烷和 CG 但烷的 1:1 混合物的性质,这些混合物应表现出理想的混合行为,我们得出结论,MARTINI 和 SB 势特别适合与原子力场结合。随后,MARTINI 势用于在 CG 但烷和水中对原子 dialanine 肽进行混合模拟。与系统的全原子描述相比,混合描述给出了相似的结果,只要考虑到水的介电屏蔽即可。在生物分子领域,我们的方法似乎非常适合研究例如蛋白质 - 配体结合,其中活性位点和配体以原子细节建模,其余的蛋白质与溶剂一起粗粒化。

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