Abstract

The antibiotic monazomycin, operated in a current-clamp mode, is shown to provide a convenient, sensitive, and continuous monitor of the interactions of charged moieties, including biological materials, with planar bilayer lipid membranes. The technique is quite general; its use is illustrated by demonstrating the interactions of phosphatidylserine vesicles, poly-L-lysine, cytochrome c, and MgSO 4 with planar lipid bilayers.

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