Effect of different treatments of long-range interactions and sampling conditions in molecular dynamic simulations of rhodopsin embedded in a dipalmitoyl phosphatidylcholine bilayer
2007 (English)In: Journal of Computational Chemistry, ISSN 0192-8651, E-ISSN 1096-987X, Vol. 28, no 6, 1017-1030 p.Article, review/survey (Refereed) Published
The present study analyzes the effect of the simulation conditions on the results of molecular dynamics simulations of G-protein coupled receptors (GPCRs) performed with an explicit lipid bilayer. Accordingly, the present work reports the analysis of different simulations of bovine rhodopsin embedded in a dipalmitoyl phosphatidylcholine (DPPC) lipid bilayer using two different sampling conditions and two different approaches for the treatment of long-range electrostatic interactions. Specifically, sampling was carried out either by using the statistical ensembles NVT or NPT (constant number of atoms, a pressure of 1 arm in all directions and fixed temperature), and the electrostatic interactions were treated either by using a twin-cutoff, or the particle mesh Ewald summation method (PME). The results of the present study suggest that the use of the NPT ensemble in combination with the PME method provide more realistic simulations. The use of NPT during the equilibration avoids the need of an a priori estimation of the box dimensions, giving the correct area per lipid. However, once the system is equilibrated, the simulations are irrespective of the sampling conditions used. The use of an electrostatic cutoff induces artifacts on both lipid thickness and the ion distribution, but has no direct effect on the protein and water molecules.
Place, publisher, year, edition, pages
2007. Vol. 28, no 6, 1017-1030 p.
molecular dynamics, lipid bilayer, simulation setup, membrane protein, rhodopsin, electrostatics, ensembles, protein-coupled receptors, membrane-mediated interactions, particle mesh ewald, lipid-bilayers, electrostatic interactions, phospholipid-bilayers, solvated polypeptides, protonation states, force-field, computer-simulations
IdentifiersURN: urn:nbn:se:kth:diva-16462DOI: 10.1002/jcc.20579ISI: 000245029500003ScopusID: 2-s2.0-33947732290OAI: oai:DiVA.org:kth-16462DiVA: diva2:334504
QC 201005252010-08-052010-08-05Bibliographically approved