Journal Title
Title of Journal: Eur Biophys J
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Abbravation: European Biophysics Journal
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Publisher
Springer-Verlag
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Authors: Anthony Ivetac Mark S P Sansom
Publish Date: 2007/10/25
Volume: 37, Issue: 4, Pages: 403-409
Abstract
Despite a growing repertoire of membrane protein structures currently ∼120 unique structures considerations of low resolution and crystallization in the absence of a lipid bilayer require the development of techniques to assess the global quality of membrane protein folds This is also the case for assessment of eg homology models of human membrane proteins based on structures of distant bacterial homologues Molecular dynamics MD simulations may be used to help evaluate the quality of a membrane protein structure or model We have used a structure of the bacterial ABC transporter MsbA which has the correct transmembrane helices but an incorrect handedness and topology of their packing to test simulation methods of quality assessment An MD simulation of the MsbA model in a lipid bilayer is compared to a simulation of another bacterial ABC transporter BtuCD The latter structure has demonstrated good conformational stability in the same bilayer environment and over the same timescale 20 ns as for the MsbA model simulation A number of comparative analyses of the two simulations were performed to assess changes in the structural integrity of each protein The results show a significant difference between the two simulations chiefly due to the dramatic structural deformations of MsbA We therefore propose that MD could become a useful quality control tool for membrane protein structural biology In particular it provides a way in which to explore the global conformational stability of a model membrane protein fold
Keywords:
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