Journal article
The Free Energy Landscape of Dimerization of a Membrane Protein, NanC
TA Dunton, JE Goose, DJ Gavaghan, MSP Sansom, JM Osborne
Plos Computational Biology | PUBLIC LIBRARY SCIENCE | Published : 2014
Abstract
Membrane proteins are frequently present in crowded environments, which favour lateral association and, on occasions, two-dimensional crystallization. To better understand the non-specific lateral association of a membrane protein we have characterized the free energy landscape for the dimerization of a bacterial outer membrane protein, NanC, in a phospholipid bilayer membrane. NanC is a member of the KdgM-family of bacterial outer membrane proteins and is responsible for sialic acid transport in E. coli. Umbrella sampling and coarse-grained molecular dynamics were employed to calculate the potentials of mean force (PMF) for a variety of restrained relative orientations of two NanC proteins ..
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Awarded by Biotechnology and Biological Sciences Research Council