Molecular simulation of multistate peptide dynamics : a comparison between microsecond timescale sampling and multiple shorter trajectories
2008 Wiley Periodicals, Inc.
Veröffentlicht in: | Journal of computational chemistry. - 1984. - 29(2008), 11 vom: 28. Aug., Seite 1740-52 |
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1. Verfasser: | |
Weitere Verfasser: | , , , |
Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2008
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Zugriff auf das übergeordnete Werk: | Journal of computational chemistry |
Schlagworte: | Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Peptides |
Zusammenfassung: | 2008 Wiley Periodicals, Inc. Molecular dynamics simulations of the RN24 peptide, which includes a diverse set of structurally heterogeneous states, are carried out in explicit solvent. Two approaches are employed and compared directly under identical simulation conditions. Specifically, we examine sampling by two individual long trajectories (microsecond timescale) and many shorter (MS) uncoupled trajectories. Statistical analysis of the structural properties indicates a qualitative agreement between these approaches. Microsecond timescale sampling gives large uncertainties on most structural metrics, while the shorter timescale of MS simulations results in slight structural memory for beta-structure starting states. Additionally, MS sampling detects numerous transitions on a relatively short timescale that are not observed in microsecond sampling, while long simulations allow for detection of a few transitions on significantly longer timescales. A correlation between the complex free energy landscape and the kinetics of the equilibrium is highlighted by principal component analysis on both simulation sets. This report highlights the increased precision of the MS approach when studying the kinetics of complex conformational change, while revealing the complementary insight and qualitative agreement offered by far fewer individual simulations on significantly longer timescales |
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Beschreibung: | Date Completed 11.08.2008 Date Revised 16.06.2008 published: Print Citation Status MEDLINE |
ISSN: | 1096-987X |
DOI: | 10.1002/jcc.20935 |