Vulnerability in Popular Molecular Dynamics Packages Concerning Langevin and Andersen Dynamics.
Vulnerability in Popular Molecular Dynamics Packages Concerning Langevin and Andersen Dynamics.
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DOI：
10.1021/ct8002173
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发表时间：
2008-10-14
影响因子：
5.5
通讯作者：
Lybrand, Terry P.
中科院分区：
文献类型：
--
作者：
Cerutti, David S.;Duke, Robert;Freddolino, Peter L.;Fan, Hao;Lybrand, Terry P.
We report a serious problem associated with a number of current implementations of Andersen and Langevin dynamics algorithms. When long simulations are run in many segments, it is sometimes possible to have a repeating sequence of pseudorandom numbers enter the calcuation. We show that, if the sequence repeats rapidly, the resulting artifacts can quickly denature biomolecules and are then easily detectable. However, if the sequence repeats less frequently, the artifacts become subtle and easily overlooked. We derive a formula for the underlying cause of artifacts in the case of the Langevin thermostat, and find it vanishes slowly as the inverse square root of the number of time steps per simulation segment. Numerous examples of simulation artifacts are presented, including dissociation of a tetrameric protein after 110 ns of dynamics, reductions in atomic fluctuations for a small protein in implicit solvent, altered thermodynamic properties of a box of water molecules, and changes in the transition free energies between dihedral angle conformations. Finally, in the case of strong thermocoupling, we link the observed artifacts to previous work in nonlinear dynamics and show that it is possible to drive a 20-residue, implicitly solvated protein into periodic trajectories if the thermostat is not used properly. Our findings should help other investigators re-evaluate simulations that may have been corrupted and obtain more accurate results.
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