Abstract

The adsorption of large unilamellar vesicles composed of various combinations of phosphatidylcholine, phosphatidylethanolamine (PE), monomethyl PE, and dimethyl PE (PE-Me 2) onto a glass surface was studied using fluorescence microscopy. The average lipid geometry within the vesicles, described mathematically by the average intrinsic curvature, C 0,ave, was methodically altered by changing the lipid ratios to determine the effect of intrinsic curvature on the ability of vesicles to rupture and form a supported lipid bilayer. We show that the ability of vesicles to create fluid planar bilayers is dependent on C 0,ave and independent of the identity of the component lipids. When the C 0,ave was ∼−0.1 nm −1, the vesicles readily formed supported lipid bilayers with almost full mobility. In contrast, when the C 0,ave ranged from ∼−0.2 to ∼−0.3 nm −1, the adsorbed vesicles remained intact upon the surface. The results indicate that the average shape of lipid molecules within a vesicle ( C 0,ave) is essential for determining kinetically viable reactions that are responsible for global geometric changes.

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