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PMID: 1532573 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cysteine 254 of the 73-kDa A subunit is responsible for inhibition of the coated vesicle (H+)-ATPase upon modification by sulfhydryl reagents.

The Journal of biological chemistry ·Vol. 267 ·No. 9 ·1992-03-25 ·Pages 5817-22

Feng Y, Forgac M

Abstract

The vacuolar class of (H+)-ATPases are highly sensitive to sulfhydryl reagents, such as N-ethylmaleimide. The cysteine residue which is responsible for inhibition of the coated vesicle (H+)-ATPase upon modification by N-ethylmalemide is located in subunit A and is able to form a disulfide bond with the cysteine moiety of cystine through an exchange reaction. This unique property distinguishes this cysteine residue from the remaining cysteine residues of the (H+)-ATPase. Using this reaction, we selectively labeled the cystine-reactive cysteine residue of subunit A with fluorescein-maleimide. After complete digestion of the labeled subunit A by V8 protease, a single labeled fragment of molecular mass 3.9 kDa was isolated and the amino-terminal sequence was determined. This fragment contains 2 cysteine residues, Cys240 and Cys254. Since Cys254 is conserved among all vacuolar (H+)-ATPases whereas Cys240 is not, it is likely that Cys254 is the residue which is responsible for the sensitivity of the vacuolar (H+)-ATPase to sulfhydryl reagents.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Brain/enzymology Cattle Clathrin/metabolism Coated Pits, Cell-Membrane/enzymology Cysteine Dithiothreitol/pharmacology Ethylmaleimide/metabolism,pharmacology Kinetics Macromolecular Substances Molecular Sequence Data Molecular Weight Proton-Translocating ATPases/antagonists & inhibitors,isolation & purification,metabolism Sulfhydryl Reagents/pharmacology
Chemicals
Clathrin Macromolecular Substances Sulfhydryl Reagents Proton-Translocating ATPases Cysteine Ethylmaleimide Dithiothreitol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Feng Y
Department of Cellular and Molecular Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
Forgac M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-03-25
Pages
5817-22
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · R01 GM034478 · United States
NIGMS NIH HHS · GM-34478 · United States
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