Structural features of a multisubstate cardiac mitoplast anion channel: inferences from single channel recording.

Ion channels from sheep cardiac mitoplast (inverted inner mitochondrial membrane vesicle) preparations were incorporated into voltage-clamped planar lipid bilayers. A low-conductance anion channel (approximately 40 or approximately 85 pS in symmetric 300 or 550 mM choline Cl, respectively), characterized by the presence of two well-defined substates, at approximately 25 and approximately 50% of the fully open level, was studied in detail. The substate behavior was consistent with a multibarelled channel containing four functionally coupled pores. At negative (cis-trans) membrane potentials, the putative protomers appeared to gate with substantial positive cooperativity, accounting for the apparent absence of a approximately 75% sublevel. At positive holding potentials, allosteric promoter interactions were more complicated, and the channel complex could be modeled as a dimer of dimers. The protochannels in one dimer ("dimer A") appeared to open independently of each other, and with a relatively high probability, while the monomers comprising the second dimer ("dimer B") were functionally coupled, could only open if both protomers in dimer A were open, and closed as soon as one of the monomers in dimer A shut. The channels also displayed Ca(2+)-(and Mg(2+)-) sensitive rectification related to bilayer lipid surface charge. By assuming that Ca2+ acted solely by screening surface charge, the membrane surface potential profile was used as a "microscopic ruler" to place one month of the channel within 10-11 A of the bilayer surface.