ATP-dependent proton uptake by proteoliposomes reconstituted with purified Na+,K+-ATPase

J Biol Chem. 1986 Sep 25;261(27):12655-8.

Abstract

Proton transport catalyzed by the sodium pump was demonstrated using proteoliposomes reconstituted with purified pig kidney Na+,K+-ATPase. Intravesicular pH was monitored with fluorescence from fluorescein isothiocyanate dextran introduced into the vesicles. An ATP-induced ouabain-sensitive acidification of the intravesicular medium was observed, when the vesicles were incubated with ATP and without Na+. The ATP-induced acidification was blocked by either extravesicular Na+ or pretreatment of the enzyme with ouabain before reconstitution. Protonophores, X-537A or carbonyl cyanide m-chlorophenylhydrazone, abolished the intravesicular acidification. The acidification was not inhibited by 3 mM tetra-n-butylammonium. The initial rate of the H+ uptake was increased with a decrease in pH of the extravesicular medium, and the maximum rate was obtained at pH 5.5-5.6. It is concluded that H+ can be transported in place of Na+ by the sodium pump.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Dextrans
  • Fluorescein-5-isothiocyanate* / analogs & derivatives*
  • Fluoresceins
  • Hydrogen-Ion Concentration
  • Kidney / enzymology
  • Membrane Potentials
  • Ouabain / pharmacology
  • Proteolipids / metabolism*
  • Protons*
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Spectrometry, Fluorescence
  • Swine

Substances

  • Dextrans
  • Fluoresceins
  • Proteolipids
  • Protons
  • fluorescein isothiocyanate dextran
  • proteoliposomes
  • Ouabain
  • Adenosine Triphosphate
  • Sodium-Potassium-Exchanging ATPase
  • Fluorescein-5-isothiocyanate