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Membrane Perturbation Induced by Interfacially Adsorbed Peptides

Assaf Zemel ^*, Avinoam Ben-Shaul ^* and Sylvio May 

^* Department of Physical Chemistry and the Fritz Haber Research Center, The Hebrew University of Jerusalem, Jerusalem 91904, Israel; and Institut für Molekularbiologie, Friedrich-Schiller-Universität Jena, 07745 Jena, Germany

Correspondence: Address reprint requests to Sylvio May, Institut für Molekularbiologie, Winzerlaer Strasse 10, 07745 Jena, Germany. Tel.: 49-3641-657582; E-mail: Silvio.May{at}uni-jena.de.

The structural and energetic characteristics of the interaction between interfacially adsorbed (partially inserted) -helical, amphipathic peptides and the lipid bilayer substrate are studied using a molecular level theory of lipid chain packing in membranes. The peptides are modeled as "amphipathic cylinders" characterized by a well-defined polar angle. Assuming two-dimensional nematic order of the adsorbed peptides, the membrane perturbation free energy is evaluated using a cell-like model; the peptide axes are parallel to the membrane plane. The elastic and interfacial contributions to the perturbation free energy of the "peptide-dressed" membrane are evaluated as a function of: the peptide penetration depth into the bilayer's hydrophobic core, the membrane thickness, the polar angle, and the lipid/peptide ratio. The structural properties calculated include the shape and extent of the distorted (stretched and bent) lipid chains surrounding the adsorbed peptide, and their orientational (C-H) bond order parameter profiles. The changes in bond order parameters attendant upon peptide adsorption are in good agreement with magnetic resonance measurements. Also consistent with experiment, our model predicts that peptide adsorption results in membrane thinning. Our calculations reveal pronounced, membrane-mediated, attractive interactions between the adsorbed peptides, suggesting a possible mechanism for lateral aggregation of membrane-bound peptides. As a special case of interest, we have also investigated completely hydrophobic peptides, for which we find a strong energetic preference for the transmembrane (inserted) orientation over the horizontal (adsorbed) orientation.

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