Conditions for liposome adsorption and bilayer formation on BSA passivated solid supports

• Formation of lipid bilayers through the adsorption of SUVs critically depends on the state of the BSA.
• Glass substrates coated with a smooth layer of native BSA will readily promote the formation of lipid bilayers.
• Glass substrates coated with a smooth layer of heat denatured or chemically reduced BSA will readily promote the adsorption of intact lipid vesicles, but will not promote the formation of lipid bilayers.
• Increasing concentrations of B-ME will swell SUVs, except those containing negatively charged lipids, but has no effect on bilayer formation.
• Reduced-Heat Denatured BSA has low solubility and will not fully coat a hydrophillically treated glass substrate, but dots the surface with nanometer sized islands, strings, and loops

Planar solid supported lipid membranes that include an intervening bovine serum albumen (BSA) cushion can greatly reduce undesirable interactions between reconstituted membrane proteins and the underlying substrate. These hetero-self-assemblies reduce frictional coupling by shielding reconstituted membrane proteins from the strong surface charge of the underlying substrate, thereby preventing them from strongly sticking to the substrate themselves. The motivation for this work is to describe the conditions necessary for liposome adsorption and bilayer formation on these hetero-self-assemblies. Described here are experiments that show that the state of BSA is critically important to whether a lipid bilayer is formed or intact liposomes are adsorbed to the BSA passivated surface. It is shown that a smooth layer of native BSA will readily promote lipid bilayer formation while BSA that has been denatured either chemically or by heat will not. Atomic force microscopy (AFM) and fluorescence microscopy was used to characterize the surfaces of native, heat denatured, and chemically reduced BSA. The mobility of several zwitterionic and negatively charged lipid combinations has been measured using fluorescence recovery after photobleaching (FRAP). From these measurements diffusion constants and percent recoveries have been determined and tabulated. The effect of high concentrations of beta-mercaptoethanol (β-ME) on liposome formation as well as bilayer formation was also explored.