Journal
CHEMISTRY AND PHYSICS OF LIPIDS
Volume 163, Issue 6, Pages 530-537Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.chemphyslip.2010.04.007
Keywords
Ion-channel; LS2 peptide; All-atom; Tetramer bundle; WALP peptide; DMPC bilayer
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Funding
- University of the Sciences in Philadelphia (USP)
- National Institute of Health [R15GM075990]
- National Science Foundation [CHE-0420556, CCF-0622162]
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The conformations of model transmembrane peptides are studied to understand the structural and dynamical aspects of tetrameric bundles using a series of coarse grain (CG) molecular dynamics (MD) simulations since membrane proteins play a crucial role in cell function. In this work, two different amphipathic models have been constructed using similar hydrophobic/hydrophilic characteristics with two structurally distinct morphologies to evaluate the effect of roughness and hydrophilic topology on the structure of tetrameric bundles, one class that forms an ion-channel and one class that does not. Free energy calculations of typical amphipathic peptide topologies show that using a relatively smooth surface morphology allows for a stable conformation of the tetramer bundle in a diamond formation. However, the model with side chains attached to the core in order to roughen the surface has a stable square tetramer bundle which is consistent with experimental data and all-atom (AA) MD simulations. Comparisons of the CG simulations with AA MD simulations are in reasonable agreement with the formation of tetrameric homo-oligomers, partitioning within the lipid bilayer and tilt angle with respect to the bilayer normal. We concluded that a square or diamond shape tetrameric homo-oligomers could be stabilized by rational design of the peptide morphology and topology of the surface, thus allowing us to tune the permeability of the bundle or channel. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
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