Résumé
Both porins OmpA1, from wild-strain K12
Escherichia coli, and OmpA2, from a K12 derivative deficient in both OmpF and OmpC, are able to form ion channels in virtually solvent-free membranes. The conductance has been shown to vary in a discrete fashion with different single increment values especially with OmpA2. This behaviour seems to indicate, beside monomers, the presence of aggregates of different sizes. The estimated small pore diameter (0.6–0.7 nm) for the monomeric would explain the weak permeability of this narrow channel toward different solutes. OmpA protein, from experiments of ion selectivity and zero-current potential, is determined weakly anion selective.