Fluorescence quenching study of melittin-membrane interactions.

The bee venom peptide melittin is a popular object for studying lipid-protein interactions. In this paper we show that binding of melittin to the bilayer is a complex process involving several steps. We were able to resolve those steps by utilizing a new approach in the quantitative analysis of depth-dependent fluorescence quenching in membranes. The "distribution analysis" technique (DA) employed here provides not only the most probable depth of the fluorophore but also allows the estimation of its conformational heterogeneity and accessibility to the lipid phase. A model for melittin interaction with the membranes is suggested.