Two methods for patterning surfaces with supported lipid bilayers and immob
ilized protein are described. First, proteins are used to fabricate corrals
for supported lipid bilayers. Poly(dimethylsiloxane) stamps are used to de
posit arbitrarily shaped patterns of thin layers of immobilized protein ont
o glass surfaces. This is followed by vesicle fusion into the regions that
are not coated with proteins. Second, supported bilayer membranes are blott
ed to remove patterned regions of the membrane,(1) and the blotted regions
are filled in or caulked with protein from solution. In both cases, the lip
id bilayer regions exhibit lateral fluidity, but each region is confined or
corralled by the protein. These two methods can be combined and used itera
tively to create arrays with increasing lateral complexity in both the fixe
d protein and mobile-supported membrane regions for biophysical studies or
cell-based assays.