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PMID: 2446615 Published · ppublish English Journal Article

Internal anion binding site and membrane potential dominate the regulation of proton pumping by the chromaffin granule ATPase.

Biochemical and biophysical research communications ·Vol. 149 ·No. 1 ·1987-11-30 ·Pages 140-4

Moriyama Y, Nelson N

Abstract

Effects of anions and membrane potential on the reconstituted proton pump from chromaffin granules were investigated. When acetate was present inside of the vesicles, ATP-dependent proton uptake was absolutely dependent on external chloride. Without external chloride, however, substantial proton uptake was observed when chloride or sulfate was present inside of the vesicles. Inside negative membrane potential drove ATP-dependent proton uptake regardless of the anion species present inside or outside of the vesicles. It is concluded that the internal anion binding site and membrane potential regulate the proton pumping activity of the ATPase.

MeSH Terms
Acetates/pharmacology Adenosine Triphosphate/pharmacology Animals Anions Binding Sites Cattle Chlorides/pharmacology Chromaffin Granules/enzymology Chromaffin System/enzymology Intracellular Membranes/enzymology Ion Channels/drug effects,metabolism Membrane Potentials Phosphates/pharmacology Proton-Translocating ATPases/metabolism Protons Sulfates/pharmacology
Chemicals
Acetates Anions Chlorides Ion Channels Phosphates Protons Sulfates Adenosine Triphosphate Proton-Translocating ATPases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Moriyama Y
Roche Institute of Molecular Biology, Roche Research Center, Nutley, New Jersey 07110.
Nelson N
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1987-11-30
Pages
140-4
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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