Subunit G of the vacuolar proton pump. Molecular characterization and functional expression

Bill P. Crider, Per Andersen, Allen E. White, Zhiming Zhou, Xinji Li, Jan P. Mattsson, Lennart Lundberg, David J. Keeling, Xiao Song Xie, Dennis K. Stone, Sheng Bin Peng

Research output: Contribution to journalArticle

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Abstract

The vacuolar type proton pump of clathrin-coated vesicles has a multisubunit ATP hydrolytic center that is peripheral to the membrane. Polypeptides present in this domain include the well characterized subunits A, B, C, D, E, and F; SFD, a dimer composed of 50- and 57-kDa polypeptides; and polypeptides termed G and H. Of these, subunits A, B, C, and E have been shown to be necessary but not sufficient for significant ATPase activity; in addition, either polypeptide G or H is also required for ATP hydrolysis (Xie, X.-S. (1996) J. Biol. Chem. 271, 30980-30985).In this study, the polypeptides G and H were purified and directly sequenced. Subsequent molecular analysis has revealed that these proteins are isoforms, which we designate G1 and G2. The cDNAs encoding the rat and bovine brain and chicken osteoclast forms of G1 have been cloned. The open reading frames of the rat and bovine clones encode hydrophilic proteins of 118 amino acids that differ at only five residues; bovine G1 has 36% identity with VMA10, a component of the proton channel of yeast. Northern blot analysis revealed a 1.0-kilobase pair transcript encoding G1 in bovine brain, kidney, heart, and spleen. The cDNA encoding bovine polypeptide H was cloned and sequenced, revealing this protein to be 64% identical to G1, constituting isoform G2. In Northern blot analysis, a single 1.7-kilobase pair transcript hybridized with a probe to G2 in brain, but not in heart, kidney, or spleen. An antibody against a bovine G1-specific domain reacts with V pump from bovine brain, kidney, and chromaffin granule, whereas an anti-G2 antibody reacts only with proton pump from brain. The bovine forms of G1 and G2 were subsequently expressed in Escherichia coli and Sf9 cells, respectively, and purified to homogeneity. Reconstitution of ATP hydrolysis was achieved by combination of recombinant subunits A, B, C, and E with either recombinant G1 or G2, demonstrating the role of these isoforms in pump function.

Original languageEnglish (US)
Pages (from-to)10721-10728
Number of pages8
JournalJournal of Biological Chemistry
Volume272
Issue number16
DOIs
StatePublished - Apr 18 1997

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Proton Pumps
Brain
Peptides
Protein Isoforms
Adenosine Triphosphate
Rats
Hydrolysis
Complementary DNA
Kidney
Pumps
Northern Blotting
Clathrin
Spleen
Antibodies
Clathrin-Coated Vesicles
Chromaffin Granules
Sf9 Cells
Dimers
Yeast
Escherichia coli

ASJC Scopus subject areas

  • Biochemistry

Cite this

Crider, B. P., Andersen, P., White, A. E., Zhou, Z., Li, X., Mattsson, J. P., ... Peng, S. B. (1997). Subunit G of the vacuolar proton pump. Molecular characterization and functional expression. Journal of Biological Chemistry, 272(16), 10721-10728. https://doi.org/10.1074/jbc.272.16.10721

Subunit G of the vacuolar proton pump. Molecular characterization and functional expression. / Crider, Bill P.; Andersen, Per; White, Allen E.; Zhou, Zhiming; Li, Xinji; Mattsson, Jan P.; Lundberg, Lennart; Keeling, David J.; Xie, Xiao Song; Stone, Dennis K.; Peng, Sheng Bin.

In: Journal of Biological Chemistry, Vol. 272, No. 16, 18.04.1997, p. 10721-10728.

Research output: Contribution to journalArticle

Crider, BP, Andersen, P, White, AE, Zhou, Z, Li, X, Mattsson, JP, Lundberg, L, Keeling, DJ, Xie, XS, Stone, DK & Peng, SB 1997, 'Subunit G of the vacuolar proton pump. Molecular characterization and functional expression', Journal of Biological Chemistry, vol. 272, no. 16, pp. 10721-10728. https://doi.org/10.1074/jbc.272.16.10721
Crider, Bill P. ; Andersen, Per ; White, Allen E. ; Zhou, Zhiming ; Li, Xinji ; Mattsson, Jan P. ; Lundberg, Lennart ; Keeling, David J. ; Xie, Xiao Song ; Stone, Dennis K. ; Peng, Sheng Bin. / Subunit G of the vacuolar proton pump. Molecular characterization and functional expression. In: Journal of Biological Chemistry. 1997 ; Vol. 272, No. 16. pp. 10721-10728.
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AU - Lundberg, Lennart

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