Coarse grain lipid-protein molecular interactions and diffusion with MsbA flippase
Coarse‐grained (CG) modeling has proven effective for simulating lipid bilayer dynamics on scales of biological interest. Modeling the dynamics of flexible membrane proteins within the bilayer, on the other hand, poses a considerable challenge due to the complexity of the folding or conformational l...
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Veröffentlicht in: | Proteins, structure, function, and bioinformatics structure, function, and bioinformatics, 2012-08, Vol.80 (9), p.2178-2190 |
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Sprache: | eng |
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Zusammenfassung: | Coarse‐grained (CG) modeling has proven effective for simulating lipid bilayer dynamics on scales of biological interest. Modeling the dynamics of flexible membrane proteins within the bilayer, on the other hand, poses a considerable challenge due to the complexity of the folding or conformational landscape. In the present work, the multiscale coarse‐graining method is applied to atomistic peptide‐lipid “soup” simulations to develop a general set of CG protein–lipid interaction potentials. The reduced model was constructed to be compatible with recent solvent‐free CG models developed for protein–protein folding and lipid–lipid model bilayer interactions. The utility of the force field was demonstrated by molecular dynamics simulation of the MsbA ABC transporter in a mixed DOPC/DOPE bilayer. An elastic network was parameterized to restrain the MsbA dimer in its open, closed and hydrolysis intermediate conformations and its impact on domain flexibility was examined. Conformational stability enabled long‐time dynamics simulation of MsbA freely diffusing in a 25 nm membrane patch. Three‐dimensional density analysis revealed that a shell of weakly bound “annular lipids” solvate the membrane accessible surface of MsbA and its internal substrate‐binding chamber. The annular lipid binding modes, along with local perturbations in head group structure, are a function of the orientation of grooves formed between transmembrane helices and may influence the alternating access mechanism of substrate entry and translocation. Proteins 2012; © 2012 Wiley Periodicals, Inc. |
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ISSN: | 0887-3585 1097-0134 |
DOI: | 10.1002/prot.24108 |