Literature DB >> 2446615

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

Y Moriyama1, N Nelson.   

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.

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Year:  1987        PMID: 2446615     DOI: 10.1016/0006-291x(87)91615-9

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

1.  Measurements of the acidification kinetics of single SynaptopHluorin vesicles.

Authors:  Kristi L Budzinski; Maxwell Zeigler; Bryant S Fujimoto; Sandra M Bajjalieh; Daniel T Chiu
Journal:  Biophys J       Date:  2011-10-05       Impact factor: 4.033

2.  cDNA sequence encoding the 16-kDa proteolipid of chromaffin granules implies gene duplication in the evolution of H+-ATPases.

Authors:  M Mandel; Y Moriyama; J D Hulmes; Y C Pan; H Nelson; N Nelson
Journal:  Proc Natl Acad Sci U S A       Date:  1988-08       Impact factor: 11.205

3.  Metabolic control of vesicular glutamate transport and release.

Authors:  Narinobu Juge; John A Gray; Hiroshi Omote; Takaaki Miyaji; Tsuyoshi Inoue; Chiaki Hara; Hisayuki Uneyama; Robert H Edwards; Roger A Nicoll; Yoshinori Moriyama
Journal:  Neuron       Date:  2010-10-06       Impact factor: 18.688

  3 in total

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