Coupling of ATP synthesis to reversal of rat liver microsomal Ca2+-ATPase

Biochemistry. 1985 Dec 17;24(26):7741-5. doi: 10.1021/bi00347a036.

Abstract

The reversal of the rat liver microsomal Ca2+-ATPase transport cycle was studied. Microsomes were loaded with 45Ca2+ (approximately 30 nmol/mg of protein) in an ATP-dependent process, and the time dependency of the microsomal 45Ca2+ efflux was determined with various ADP and inorganic phosphate (Pi) concentrations. Pseudo-first-order rate constants (K'e) for 45Ca2+ efflux were determined. Although there was considerable 45Ca2+ efflux in the absence of added ADP or Pi, the addition of ADP or Pi alone had minimal effects upon the K'e; in contrast, a 2.5-fold increase in the K'e was observed in the presence of both ADP and Pi. The apparent Km values for ADP and Pi were 4 microM and 0.22 mM, respectively. Stimulation of 45Ca2+ efflux by ADP and Pi was associated with ATP synthesis. The calcium ionophore A23187 prevented ATP synthesis, which indicates that the Ca2+ gradient facilitates the coupling of ATP synthesis to Ca2+ efflux.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / biosynthesis*
  • Animals
  • Biological Transport, Active
  • Calcium / metabolism
  • Calcium-Transporting ATPases / metabolism*
  • In Vitro Techniques
  • Kinetics
  • Male
  • Microsomes, Liver / metabolism*
  • Phosphates / metabolism
  • Rats

Substances

  • Phosphates
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Calcium-Transporting ATPases
  • Calcium