CHARGE PAIR INTERACTIONS STABILIZING FERREDOXIN-FERREDOXIN REDUCTASE COMPLEXES - IDENTIFICATION BY COMPLEMENTARY SITE-SPECIFIC MUTATIONS

Ferredoxin reductase (Fd-reductase) supplies electrons to mitochondria l steroid hydroxylase cytochrome P450 enzymes via a 2Fe-2S! ferredoxi n. Chemical labeling studies with bovine Fd-reductase have implicated Lys-243 as important in binding to bovine ferredoxin (Hamamoto, I., Ka zutaka, K., Tanaka, S., and Ichikawa, Y. (1988) Biochim. Biophys. Acta 953, 207-213). We have used site-directed mutagenesis to examine the role of charged residues in this region of human Fd-reductase in ferre doxin binding. Mutant proteins were expressed in Escherichia coli and were assayed for activity by ferredoxin-mediated electron transfer to cytochrome c. Replacement of Lys-242 (homologous to Lys-243 in bovine Fd-reductase) with Gln and replacement of Arg-241 with Ser had little effect (2.7- and 3.6-fold increased K(m), respectively). In contrast, mutants at positions 239 and 243 (R239S and R243Q) exhibited markedly lower affinity for ferredoxin (17.5- and 1,600-fold increased K(m), re spectively). Studies were also carried out with two ferredoxin charge mutants shown previously to have lowered affinity for Fd-reductase (Co ghlan, V. M., and Vickery, L. E. (1991) J. Biol. Chem. 266, 18606-1861 2). Comparisons of the binding of ferredoxin mutants D76N and D79N to Fd-reductase mutants R239S and R243Q suggest that Arg-239 and Arg-243 of Fd-reductase each interact directly with both Asp-76 and Asp-79 of ferredoxin during formation of the complex between the two proteins. T hese results support the hypothesis that specific electrostatic intera ctions involving this region are important in stabilizing the ferredox in-Fd-reductase complex.