The multiple nicotinamide nucleotide-binding subunits of bovine heart mitochondrial NADH:ubiquinone oxidoreductase (complex I).

Direct photoaffinity labeling of purified bovine heart NADH:ubiquinone oxidoreductase (complex I) with 32P-labeled NAD(H), NADP(H) and ADP has shown that five polypeptides become labeled, with molecular masses of 51, 42, 39, 30, and 18-20 kDa. The 51 and the 30-kDa polypeptides were labeled with either 32P]NAD(H), 32P]NADP(H) or beta-32P]ADP. The 42-kDa polypeptide was labeled with 32P]NAD(H) and to a small extent with beta-32P]ADP. It was not labeled with 32P]NADP(H). The 39-kDa polypeptide was labeled with 32P]NADPH and to a small extent with beta-32P]ADP. Our previous studies had shown that this subunit also binds NADP, but not NAD(H) Yamaguchi, M., Belogrudov, G.I. & Hatefi, Y. (1998) J. Biol. Chem. 273, 8094-8098]. The 18-20-kDa polypeptide was labeled only with 32P]NADPH. Among these polypeptides, the 51-kDa subunit is known to contain FMN and a 4Fe-4S] cluster, and is the NAD(P)H-binding subunit of the primary dehydrogenase domain of complex I. The possible roles of the other nucleotide-binding subunits of complex I have been discussed.