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PMID: 12482875 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The first putative transmembrane segment of subunit c" (Vma16p) of the yeast V-ATPase is not necessary for function.

The Journal of biological chemistry ·Vol. 278 ·No. 8 ·2003-02-21 ·Pages 5821-7

Nishi T, Kawasaki-Nishi S, Forgac M

Abstract

The yeast vacuolar ATPase (V-ATPase) contains three proteolipid subunits: c (Vma3p), c' (Vma11p), and c" (Vma16p). Each subunit contains a buried glutamate residue that is essential for function, and these subunits are not able to substitute for each other in supporting activity. Subunits c and c' each contain four putative transmembrane segments (TM1-4), whereas subunit c" is predicted to contain five. To determine whether TM1 of subunit c" serves an essential function, a deletion mutant of Vma16p was constructed lacking TM1 (Vma16p-Delta TM1). Although this construct does not complement the loss of Vma3p or Vma11p, it does complement the loss of full-length Vma16p. Vacuoles isolated from the strain expressing Vma16p-Delta TM1 showed V-ATPase activity and proton transport greater than 80% relative to wild type and displayed wild type levels of subunits A and a, suggesting normal assembly of the V-ATPase complex. These results suggest that TM1 of Vma16p is dispensable for both activity and assembly of the V-ATPase. To obtain information about the topology of Vma16p, labeling of single cysteine-containing mutants using the membrane-permeable reagent 3-(N-maleimidylpropionyl)biocytin (MPB) and the -impermeable reagent 4-acetamido-4'-maleimidylstilbene-2,2'-disulfonic acid (AMS) was tested. Both the Cys-less form of Vma16p and eight single cysteine-containing mutants retained greater than 80% of wild type levels of activity. Of the eight mutants tested, two (S5C and S178C) were labeled by MPB. MPB-labeling of S5C was blocked by AMS in intact vacuoles, whereas S178C was blocked by AMS only in the presence of permeabilizing concentrations of detergent. In addition, a hemagglutinin epitope tag introduced into the C terminus of Vma16p was recognized by an anti-hemagglutinin antibody in intact vacuolar membranes, suggesting a cytoplasmic orientation for the C terminus. These results suggest that subunit c" contains four rather than five transmembrane segments with both the N and C terminus on the cytoplasmic side of the membrane.

MeSH Terms
Amino Acid Sequence Amino Acid Substitution Molecular Sequence Data Mutagenesis, Site-Directed Protein Subunits/chemistry,metabolism Proteolipids/chemistry,metabolism Proton-Translocating ATPases/chemistry,metabolism Recombinant Proteins/chemistry,metabolism Saccharomyces cerevisiae/enzymology Saccharomyces cerevisiae Proteins/chemistry,metabolism Sequence Alignment Sequence Homology, Amino Acid Vacuolar Proton-Translocating ATPases/chemistry,metabolism
Chemicals
Protein Subunits Proteolipids Recombinant Proteins Saccharomyces cerevisiae Proteins VMA11 protein, S cerevisiae Vacuolar Proton-Translocating ATPases Proton-Translocating ATPases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nishi Tsuyoshi
Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Kawasaki-Nishi Shoko
Forgac Michael
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2003-02-21
Epub
2002-00-12
Pages
5821-7
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · R01 GM034478 · United States
NIGMS NIH HHS · R37 GM034478 · United States
NIDDK NIH HHS · DK34928 · United States
NIGMS NIH HHS · GM34478 · United States
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