Please use this identifier to cite or link to this item: https://doi.org/10.1089/10665270360688011
Title: Stochastic Roadmap Simulation: An Efficient Representation and Algorithm for Analyzing Molecular Motion
Authors: Apaydin, M.S.
Brutlag, D.L.
Guestrin, C.
Hsu, D. 
Latombe, J.-C.
Varma, C.
Keywords: Computational mutagenesis
Ligand-protein binding
Monte Carlo simulation
Probability of folding (Pfold)
Protein folding
Issue Date: 2003
Citation: Apaydin, M.S., Brutlag, D.L., Guestrin, C., Hsu, D., Latombe, J.-C., Varma, C. (2003). Stochastic Roadmap Simulation: An Efficient Representation and Algorithm for Analyzing Molecular Motion. Journal of Computational Biology 10 (3-4) : 257-281. ScholarBank@NUS Repository. https://doi.org/10.1089/10665270360688011
Abstract: Classic molecular motion simulation techniques, such as Monte Carlo (MC) simulation, generate motion pathways one at a time and spend most of their time in the local minima of the energy landscape defined over a molecular conformation space. Their high computational cost prevents them from being used to compute ensemble properties (properties requiring the analysis of many pathways). This paper introduces stochastic roadmap simulation (SRS) as a new computational approach for exploring the kinetics of molecular motion by simultaneously examining multiple pathways. These pathways are compactly encoded in a graph, which is constructed by sampling a molecular conformation space at random. This computation, which does not trace any particular pathway explicitly, circumvents the local-minima problem. Each edge in the graph represents a potential transition of the molecule and is associated with a probability indicating the likelihood of this transition. By viewing the graph as a Markov chain, ensemble properties can be efficiently computed over the entire molecular energy landscape. Furthermore, SRS converges to the same distribution as MC simulation. SRS is applied to two biological problems: computing the probability of folding, an important order parameter that measures the "kinetic distance" of a protein's conformation from its native state; and estimating the expected time to escape from a ligand-protein binding site. Comparison with MC simulations on protein folding shows that SRS produces arguably more accurate results, while reducing computation time by several orders of magnitude. Computational studies on ligand-protein binding also demonstrate SRS as a promising approach to study ligand-protein interactions.
Source Title: Journal of Computational Biology
URI: http://scholarbank.nus.edu.sg/handle/10635/40150
ISSN: 10665277
DOI: 10.1089/10665270360688011
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