Using correlated motions to determine sufficient sampling times for molecular dynamics

被引:0
|
作者
Melvin, Ryan L. [1 ,2 ]
Xiao, Jiajie [1 ,3 ]
Berenhaut, Kenneth S. [2 ]
Godwin, Ryan C. [1 ]
Salsbury, Freddie R., Jr. [1 ]
机构
[1] Wake Forest Univ, Dept Phys, 1834 Wake Forest Rd, Winston Salem, NC 27109 USA
[2] Wake Forest Univ, Dept Math & Stat, 1834 Wake Forest Rd, Winston Salem, NC 27109 USA
[3] Wake Forest Univ, Dept Comp Sci, 1834 Wake Forest Rd, Winston Salem, NC 27109 USA
基金
美国国家卫生研究院;
关键词
EMPIRICAL FORCE-FIELD; ZINC-FINGER; NUCLEIC-ACIDS; SIMULATIONS; BINDING; DNA; ALGORITHM; STABILIZATION; STABILITY; COMPLEXES;
D O I
10.1103/PhysRevE.98.023307
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Here we present a time-dependent correlation method that provides insight into how long a system takes to grow into its equal-time (Pearson) correlation. We also show a usage of an extant time-lagged correlation method that indicates the time for parts of a system to become decorrelated, relative to equal-time correlation. Given a completed simulation (or set of simulations), these tools estimate (i) how long of a simulation of the same system would be sufficient to observe the same correlated motions, (ii) if patterns of observed correlated motions indicate events beyond the timescale of the simulation, and (iii) how long of a simulation is needed to observe these longer timescale events. We view this method as a decision-support tool that will aid researchers in determining necessary sampling times. In principle, this tool is extendable to any multidimensional time series data with a notion of correlated fluctuations; however, here we limit our discussion to data from molecular-dynamics simulations.
引用
收藏
页数:7
相关论文
共 50 条