Solt, I and Kulhánek, P and Simon, I and Winfield, S and Payne, MC and Csányi, G and Fuxreiter, M (2009) Evaluating boundary dependent errors in QM/MM simulations. J Phys Chem B, 113. pp. 5728-5735. ISSN 1520-6106Full text not available from this repository.
Hybrid quantum mechanics/molecular mechanics (QM/MM) simulations provide a powerful tool for studying chemical reactions, especially in complex biochemical systems. In most works to date, the quantum region is kept fixed throughout the simulation and is defined in an ad hoc way based on chemical intuition and available computational resources. The simulation errors associated with a given choice of the quantum region are, however, rarely assessed in a systematic manner. Here we study the dependence of two relevant quantities on the QM region size: the force error at the center of the QM region and the free energy of a proton transfer reaction. Taking lysozyme as our model system, we find that in an apolar region the average force error rapidly decreases with increasing QM region size. In contrast, the average force error at the polar active site is considerably higher, exhibits large oscillations and decreases more slowly, and may not fall below acceptable limits even for a quantum region radius of 9.0 A. Although computation of free energies could only be afforded until 6.0 A, results were found to change considerably within these limits. These errors demonstrate that the results of QM/MM calculations are heavily affected by the definition of the QM region (not only its size), and a convergence test is proposed to be a part of setting up QM/MM simulations.
|Uncontrolled Keywords:||Computer Simulation Models, Chemical Models, Molecular Muramidase Quantum Theory Reproducibility of Results Thermodynamics|
|Divisions:||Div C > Materials Engineering|
|Depositing User:||Cron Job|
|Date Deposited:||28 Oct 2011 16:39|
|Last Modified:||20 May 2013 01:30|
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