Molecular dynamics simulations reveal ligand-controlled positioning of a peripheral protein complex in membranes

Steven M. Ryckbosch, Paul A. Wender () and Vijay S. Pande ()
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Steven M. Ryckbosch: Stanford University
Paul A. Wender: Stanford University
Vijay S. Pande: Stanford University

Nature Communications, 2017, vol. 8, issue 1, 1-10

Abstract: Abstract Bryostatin is in clinical trials for Alzheimer’s disease, cancer, and HIV/AIDS eradication. It binds to protein kinase C competitively with diacylglycerol, the endogenous protein kinase C regulator, and plant-derived phorbol esters, but each ligand induces different activities. Determination of the structural origin for these differing activities by X-ray analysis has not succeeded due to difficulties in co-crystallizing protein kinase C with relevant ligands. More importantly, static, crystal-lattice bound complexes do not address the influence of the membrane on the structure and dynamics of membrane-associated proteins. To address this general problem, we performed long-timescale (400–500 µs aggregate) all-atom molecular dynamics simulations of protein kinase C–ligand–membrane complexes and observed that different protein kinase C activators differentially position the complex in the membrane due in part to their differing interactions with waters at the membrane inner leaf. These new findings enable new strategies for the design of simpler, more effective protein kinase C analogs and could also prove relevant to other peripheral protein complexes.

Date: 2017
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DOI: 10.1038/s41467-016-0015-8

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