Incorporation of membrane proteins into large single bilayer vesicles. Application to rhodopsin.

Abstract

A general procedure to incorporate membrane proteins in a native state into large single bilayer vesicles is described. The results obtained with rhodopsin from vertebrate and invertebrate retinas are presented. The technique involves: the direct transfer of rhodopsin-lipid complexes from native membranes into ether or pentane, and the sonication of the complex in apolar solvent with aqueous buffer followed by solvent evaporation under reduced pressure. The spectral properties of rhodopsin in the large vesicles are similar to those of rhodopsin in photoreceptors; furthermore, bleached bovine rhodopsin is chemically regenerable with 9-cis-retinal. The presence of photochemically functional rhodopsin in the large vesicles is established. Freeze-fracture replicas of the vesicles reveal that both internal and external leaflets contain numerous particles .apprx. 80 .ANG. in diameter, indicating that rhodopsin is symmetrically distributed within the bilayer. More than 75% of the membrane area is incorporated into vesicles larger than 0.5 .mu.m and .apprx. 40% into vesicles larger than 1 .mu.m.