LYSOLIPID EXCHANGE WITH LIPID VESICLE MEMBRANES

While the aqueous solubility for bilayer phospholipids is less than 10(-10) M-keeping lipid membranes at essentially constant mass, single chain surfactants can have a significant aqueous solubility. Thus, in surfactant solutions, both monomer and micelles can interact with a lipid bilayer, and the mass and composition of the bilayer can be changed in seconds. These changes in composition are expected to have direct consequences on bilayer structure and material properties. We have found that the exchange of surfactants like lysolecithin can be described in terms of a kinetic model in which monomer and micelles are transported to the membrane from bulk solution. Molecular transport is considered at the membrane interfaces and across the midplane between the two monolayers of the bilayer. Using micropipet manipulation, single vesicles were transferred into lysolecithin solutions, and the measurement of vesicle area change gave a direct measure of lysolecithin uptake. Transfer back to lysolecithin-free media resulted in desorption. The rates of uptake and desorption could therefore be measured at controlled levels of membrane stress. With increasing lysolecithin concentration in the bulk phase, the amount of lysolecithin in the membrane reached saturation at similar to 3 mol% for concentrations below the critical micelle concentration (CMC) and at >30 mol% for concentrations above the CMC. When convective transport was used to deliver lysolecithin, uptake occurred via a double exponential: initial uptake into the outer monolayer was fast (similar to 0.2 sec(-1)); transfer across the bilayer midplane was much slower (0.0019 sec(-1)).