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Biophys J, December 2000, p. 3201-3216, Vol. 79, No. 6
Department of Physics, University of Guelph, Guelph, Ontario N1G 2W1, Canada
A molecular dynamics simulation of a fully hydrated model
membrane consisting of 12 molecules of
1,2-dimyristoyl-sn-glycero-3-phosphocholine, one
amphiphilic peptide with the sequence
acetyl-Lys-Lys-Gly-Leu16-Lys-Lys-Ala-amide, and 593 water
molecules was performed for 1.06 ns (Belohorcova, K., J. H. Davis,
T. B. Woolf, and B. Roux. 1997. Biophys. J.
73:3039-3055). The analysis presented here is primarily focused on the
phospholipid component and the results are compared with experimental
2H-NMR studies of the lipid component of mixtures of the
same peptide and lipid at a molar ratio of 1:32, and with earlier
studies of closely related peptide/lipid mixtures. The phospholipid
chain and headgroup isomer populations and isomerization rates compare favorably with previous simulations and experimental measurements. Of
particular interest is the effect of the peptide on the phospholipid headgroup and hydrocarbon chain orientational order calculated from the
simulation, which also agree well with experimental measurements performed on this and closely related systems. Comparison of the experimental results with the simulations not only shows that there is
significant agreement between the two methods, but also provides new
insight into the effect of the peptide on the lipid dynamics. In
particular, these results confirm that a membrane spanning peptide has
little effect on lipid chain order, and bilayer thickness if its
hydrophobic length closely matches the lipid hydrocarbon thickness. In
addition, we find that the peptide can have a strong ordering effect if
it is longer than the lipid hydrophobic thickness.
Biophys J, December 2000, p. 3201-3216, Vol. 79, No. 6
© 2000 by the Biophysical Society 0006-3495/00/12/3201/16 $2.00
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