Cholesterol attenuates the interaction of the antimicrobial peptide gramicidin S with phospholipid bilayer membranes

• Published in: Biochimica et biophysica acta Vol. 1510; no. 1-2; pp. 83 - 92
• Main Authors: Prenner, E J, Lewis, R N, Jelokhani-Niaraki, M, Hodges, R S, McElhaney, R N
• Format: Journal Article
• Language: English
• Published: Netherlands 09.02.2001
• Subjects: Anti-Bacterial Agents - chemistry; Cholesterol - pharmacology; Circular Dichroism; Drug Interactions; Gramicidin - chemistry; Lipid Bilayers - chemistry; Magnetic Resonance Spectroscopy; Phospholipids - chemistry; Protein Conformation; Spectroscopy, Fourier Transform Infrared
• ISSN: 0006-3002; 0005-2736; 1878-2434
• DOI: 10.1016/S0005-2736(00)00337-0

We have investigated the effect of the presence of 25 mol percent cholesterol on the interactions of the antimicrobial peptide gramicidin S (GS) with phosphatidylcholine and phosphatidylethanolamine model membrane systems using a variety of methods. Our circular dichroism spectroscopic measurements indicate that the incorporation of cholesterol into egg phosphatidylcholine vesicles has no significant effect on the conformation of the GS molecule but that this peptide resides in a range of intermediate polarity as compared to aqueous solution or an organic solvent. Our Fourier transform infrared spectroscopic measurements confirm these findings and demonstrate that in both cholesterol-containing and cholesterol-free dimyristoylphosphatidylcholine liquid-crystalline bilayers, GS is located in a region of intermediate polarity at the polar--nonpolar interfacial region of the lipid bilayer. However, GS appears to be located in a more polar environment nearer the bilayer surface when cholesterol is present. Our (31)P-nuclear magnetic resonance studies demonstrate that the presence of cholesterol markedly reduces the tendency of GS to induce the formation of inverted nonlamellar phases in model membranes composed of an unsaturated phosphatidylethanolamine. Finally, fluorescence dye leakage experiments indicate that cholesterol inhibits the GS-induced permeabilization of phosphatidylcholine vesicles. Thus in all respects the presence of cholesterol attenuates but does not abolish the interactions of GS with, and the characteristic effects of GS on, phospholipid bilayers. These findings may explain why it is more potent at disrupting cholesterol-free bacterial than cholesterol-containing eukaryotic membranes while nevertheless disrupting the integrity of the latter at higher peptide concentrations. This additional example of the lipid specificity of GS may aid in the rational design of GS analogs with increased antibacterial but reduced hemolytic activities.