The mechanism of superoxide production by the antimycin-inhibited mitochondrial Q-cycle

Abstract

Superoxide production from antimycin-inhibited complex III in isolated mitochondria first increased to a maximum then decreased as substrate supply was modulated in three different ways. In each case, superoxide production had a similar bell-shaped relationship to the reduction state of cytochrome b 566, suggesting that superoxide production peaks at intermediate Q-reduction state because it comes from a semiquinone in the outer quinone-binding site in complex III (Q o). Imposition of a membrane potential changed the relationships between superoxide production and b 566 reduction and between b 562 and b 566 redox states, suggesting that b 562 reduction also affects semiquinone concentration and superoxide production. To assess whether this behavior was consistent with the Q-cycle mechanism of complex III, we generated a kinetic model of the antimycin- inhibited Q o site. Using published rate constants (determined without antimycin), with unknown rate constants allowed to vary, the model failed to fit the data. However, when we allowed the rate constant for quinol oxidation to decrease 1000-fold and the rate constant for semiquinone oxidation by b 566 to depend on the b 562 redox state, the model fit the energized and de-energized data well. In such fits, quinol oxidation was much slower than literature values and slowed further when b 566 was reduced, and reduction of b 562 stabilized the semiquinone when b566 was oxidized. Thus, superoxide production at Q o depends on the reduction states of b 566 and b 562 and fits the Q-cycle only if particular rate constants are altered when b oxidation is prevented by antimycin. These mechanisms limit superoxide production and short circuiting of the Q-cycle when electron transfer slows. © 2011 by The American Society for Biochemistry and Molecular Biology, Inc.