Quantifying artifacts in Ewald simulations of inhomogeneous systems with a net charge
Hub, J. S., De Groot, B. L., Grubmüller, H., & Groenhof, G. (2014). Quantifying artifacts in Ewald simulations of inhomogeneous systems with a net charge. Journal of Chemical Theory and Computation, 10(1), 381-390. https://doi.org/10.1021/ct400626b
Published in
Journal of Chemical Theory and ComputationDate
2014Discipline
Epäorgaaninen ja analyyttinen kemiaNanoscience CenterInorganic and Analytical ChemistryNanoscience CenterCopyright
© 2013 American Chemical Society
Ewald summation, which has become the
de facto
standard for computing electrostatic interactions in biomolecular
simulations, formally requires that the simulation box is neutral. For non-neutral systems the Ewald algorithm
implicitly introduces a uniform background charge distribution that e ectively neutralizes the simulation box.
Because a uniform distribution of counter charges typically deviates from the spatial distribution of counterions in
real systems, artifacts may arise, in particular in systems with an inhomogeneous dielectric constant. Here we derive
an analytical expression for the e ect of using an implicit background charge instead of explicit counterions, on
the chemical potential of ions in heterogeneous systems, which (i) provides a quantitative criterium for deciding if
the background charge o ers an acceptable trade-o between artifacts arising from sampling problems and artifacts
arising from the homogeneous background charge distribution; and (ii) can be used to correct this artifact in
certain cases. Because the artifact is due to the
di erence
in charge density between the non-neutral system with a
uniform neutralizing background charge and the real neutral system with a physically correct distribution of explicit
counterions, our model quanti es the artifact in terms of this di erence. We show that for inhomogeneous systems,
such as proteins and membranes in water, the artifact manifests itself by an overstabilization of ions inside the lower
dielectric by tens to even hundreds kilojoules per mole. We have tested the accuracy of our model in molecular
dynamics simulations and found that the error in the calculated free energy for moving a test charge from water into a hexadecane/water slab at di erent net charges of the system and di erent simulation box sizes, is correctly
predicted by the model, con rming that the incorrect distribution of counter charges in the simulation box is solely
responsible for the errors in the PMFs.
...
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American Chemical SocietyISSN Search the Publication Forum
1549-9618Keywords
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https://converis.jyu.fi/converis/portal/detail/Publication/23652563
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