Genetic fusions of subunit c in the F0 sector of H+-transporting ATP synthase -: Functional dimers and trimers and determination of stoichiometry by cross-linking analysis

The multicopy c subunit of the H+-transporting ATP synthase of Escherichia coli folds through the transmembrane F-0 sector as a hairpin of two hydrophobic alpha-helices with the proton-translocating aspartyl-61 side chain centered in the second transmembrane helix. The number of subunits c in the F-0 complex, which is thought to determine the H+-pumping/ATP stoichiometry, was previously not determined with exactness but thought to range from 9-12. The studies described here indicate that the exact number is 12. Based upon the precedent of the subunit c in vacuolar-type ATPases, which are composed of four transmembrane helices and seem to have evolved by gene duplication of an F-0-type progenitor gene, we constructed genetically fused dimers and trimers off. coli subunit c. Both the dimeric and trimeric forms proved to be functional. These results indicate that the total number of subunit c in F-0 should be a multiple of 2 and 3. Based upon a previous study in which the oligomeric organization of c subunits in F-0 was determined by cross-linking of Cys-substituted subunits (Jones, P. C., Jiang, W., and Fillingame, R. H. (1998) J. Biol. Chem. 273, 17178-17185), we introduced Cys into the first and last transmembrane helices of subunit c monomers, dimers, and trimers and attempted to generate cross-linked products by oxidation with Cu(II)-(1,10-phenanthroline)(2). Double Cys substitutions at two sets of positions gave rise to extensive cross linked multimers. Multimers of the monomer that extended up to the position of c(12) were correlated and calibrated with distinct cross-linked species of the appropriate doubly Cys-substituted dimers (i.e. c(2), c(4)...c(12)) and doubly Cys-substituted trimers (i.e. c(3), c(6), c(9), c(12)). The results show that there are 12 copies of subunit c per F-0 in E. coli, the exact number having both mechanistic and structural significance.