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自适应多尺度算法,用于高效模拟拥挤条件下的多蛋白系统。

Self-adaptive multiscaling algorithm for efficient simulations of many-protein systems in crowded conditions.

机构信息

Center for Molecular Modeling, OIR/CIT, National Institutes of Health, U.S. DHHS, USA.

出版信息

Phys Chem Chem Phys. 2018 Nov 21;20(45):28544-28557. doi: 10.1039/c8cp05517c.

Abstract

A method is described for the efficient simulation of multiprotein systems in crowded environments. It is based on an adaptive, reversible structural coarsening algorithm that preserves relevant physical features of the proteins across scales. Water is treated implicitly whereas all the other components of the aqueous solution, such as ions, cosolutes, or osmolytes, are treated in atomic detail. The focus is on the analytical adaptation of the solvent model to different levels of molecular resolutions, which allows continuous, on-the-fly transitions between scales. This permits the analytical calculation of forces during dynamics and preserves detailed balance in Monte Carlo simulations. A major computational speedup can be achieved in systems containing hundreds of proteins without cutting off the long-range interactions. The method can be combined with a self-adaptive configurational-bias sampling technique described previously, designed to detect strong, weak, or ultra-weak protein associations and shown to improve sampling efficiency and convergence. The implementation aims to simulate early stages of multimeric complexation, aggregation, or self-assembly. The method can be adopted as the basis for a more general algorithm to identify vertices, edges, and hubs in protein interaction networks or to predict critical steps in signal transduction pathways.

摘要

本文描述了一种在拥挤环境中有效模拟多蛋白系统的方法。它基于一种自适应、可逆的结构粗化算法,该算法在跨尺度的情况下保留了蛋白质的相关物理特征。水是隐式处理的,而水溶液中的所有其他成分,如离子、共溶剂或渗透物,都是以原子细节处理的。重点是将溶剂模型分析性地适应于不同的分子分辨率水平,从而允许在尺度之间进行连续的、实时的转换。这允许在动力学过程中分析计算力,并在蒙特卡罗模拟中保持详细平衡。在包含数百种蛋白质的系统中,可以实现显著的计算速度提升,而不会切断长程相互作用。该方法可以与之前描述的自适应构象偏差采样技术相结合,该技术旨在检测强、弱或超弱蛋白质相互作用,并且已被证明可以提高采样效率和收敛性。该实现旨在模拟多聚体复合、聚集或自组装的早期阶段。该方法可以作为识别蛋白质相互作用网络中的顶点、边和枢纽,或预测信号转导途径中关键步骤的更通用算法的基础。

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本文引用的文献

1
Programmable protein circuits in living cells.
Science. 2018 Sep 21;361(6408):1252-1258. doi: 10.1126/science.aat5062.
2
Multiplexed protein maps link subcellular organization to cellular states.
Science. 2018 Aug 3;361(6401). doi: 10.1126/science.aar7042.
4
Binding kinetics of ultrasmall gold nanoparticles with proteins.
Nanoscale. 2018 Feb 15;10(7):3235-3244. doi: 10.1039/c7nr06810g.
5
Detection principles of biological and chemical FET sensors.
Biosens Bioelectron. 2017 Dec 15;98:437-448. doi: 10.1016/j.bios.2017.07.010. Epub 2017 Jul 5.
6
Computational Study of the Forces Driving Aggregation of Ultrasmall Nanoparticles in Biological Fluids.
ACS Nano. 2017 Apr 25;11(4):4145-4154. doi: 10.1021/acsnano.7b00981. Epub 2017 Mar 21.
7
Computational study of the inhibitory mechanism of the kinase CDK5 hyperactivity by peptide p5 and derivation of a pharmacophore.
J Comput Aided Mol Des. 2016 Jun;30(6):513-21. doi: 10.1007/s10822-016-9922-3. Epub 2016 Jul 8.
8
A Microfluidic Platform for Real-Time Detection and Quantification of Protein-Ligand Interactions.
Biophys J. 2016 May 10;110(9):1957-66. doi: 10.1016/j.bpj.2016.03.038.
10
Modeling and simulation of protein-surface interactions: achievements and challenges.
Q Rev Biophys. 2016;49:e4. doi: 10.1017/S0033583515000256.

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