valinomycin and butyltriphenylphosphonium

Equilibration of the butyltriphenyl phosphonium (BTPP+) cation into cytochrome c oxidase reconstituted proteoliposomes was measured potentiometrically. The maximum membrane potential (delta psi) generated by oxidase activity was estimated to lie between -65 and -90 mV, vesicle interior negative, when internal BTPP+ binding is taken into account. Formation of delta psi was completely prevented by valinomycin and carbonyl-cyanide-p-trifluoromethoxyphenylhydrazone but only 10% inhibited by levels of N',N'-dicyclohexylcarbodiimide that abolish proton pumping by the oxidase. delta psi is thus maintained by at least one charge transfer process that does not involve proton movement. A nonlinear relationship was obtained between oxidase activity and steady-state delta psi. The value of delta psi estimated by BTPP+ distribution was lower than that calculated using the optical probes safranine and a carbocyanine dye. Possible reasons for this discrepancy are discussed.

Topics: Animals; Azides; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Cattle; Dicyclohexylcarbodiimide; Electrodes; Electron Transport Complex IV; Energy Metabolism; Liposomes; Membrane Potentials; Nigericin; Onium Compounds; Organophosphorus Compounds; Sodium Azide; Valinomycin