A molecular simulation protocol to avoid sampling redundancy and discover new states

TitleA molecular simulation protocol to avoid sampling redundancy and discover new states
Publication TypeJournal Article
Year of Publication2015
AuthorsBacci M., Vitalis A., Caflisch A.
JournalBiochimica et Biophysica Acta (BBA) - General Subjects
Volume1850
Issue5
Pagination889-902
Date Published2015 May
Type of ArticleResearch Article
ISSN0006-3002
KeywordsBiomolecules, Enhanced sampling, molecular dynamics, Scalable algorithm, Simulation convergence, Transition path
Abstract

BACKGROUND: For biomacromolecules or their assemblies, experimental knowledge is often restricted to specific states. Ambiguity pervades simulations of these complex systems because there is no prior knowledge of relevant phase space domains, and sampling recurrence is difficult to achieve. In molecular dynamics methods, ruggedness of the free energy surface exacerbates this problem by slowing down the unbiased exploration of phase space. Sampling is inefficient if dwell times in metastable states are large.

METHODS: We suggest a heuristic algorithm to terminate and reseed trajectories run in multiple copies in parallel. It uses a recent method to order snapshots, which provides notions of "interesting" and "unique" for individual simulations. We define criteria to guide the reseeding of runs from more "interesting" points if they sample overlapping regions of phase space.

RESULTS: Using a pedagogical example and an α-helical peptide, the approach is demonstrated to amplify the rate of exploration of phase space and to discover metastable states not found by conventional sampling schemes. Evidence is provided that accurate kinetics and pathways can be extracted from the simulations.

CONCLUSIONS: The method, termed PIGS for Progress Index Guided Sampling, proceeds in unsupervised fashion, is scalable, and benefits synergistically from larger numbers of replicas. Results confirm that the underlying ideas are appropriate and sufficient to enhance sampling.

GENERAL SIGNIFICANCE: In molecular simulations, errors caused by not exploring relevant domains in phase space are always unquantifiable and can be arbitrarily large. Our protocol adds to the toolkit available to researchers in reducing these types of errors. This article is part of a Special Issue entitled "Recent Developments of Molecular Dynamics."

DOI10.1016/j.bbagen.2014.08.013
pubindex

0196

Alternate JournalBiochim. Biophys. Acta
PubMed ID25193737