Characterization of phosphotyrosyl-protein phosphatase activity associated with calcineurin

Biochem Biophys Res Commun. 1984 May 31;121(1):141-8. doi: 10.1016/0006-291x(84)90698-3.

Abstract

Calcineurin purified from bovine brain is shown to possess phosphotyrosyl -protein phosphatase activity towards proteins phosphorylated by the epidermal growth factor receptor/kinase. The phosphatase activity is augmented by Ca2+/calmodulin or divalent cation (Ni2+ greater than Mn2+ greater than Mg2+ greater than Co2+). In the simultaneous presence of all three effectors, the enzymatic activity is synergistically increased. Ca2+/calmodulin activates the Mg2+-supported activity by decreasing the Km value for phosphotyrosyl -casein from 2.2 to 0.6 microM, and increasing the Vmax from 0.4 to 4.6 nmol/min/mg. These results represent the first demonstration that calcineurin can dephosphorylate phosphotyrosyl -proteins and suggest a novel mechanism of activation of this enzyme.

Publication types

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

MeSH terms

  • Animals
  • Brain / enzymology
  • Calcium / physiology
  • Calmodulin / physiology
  • Calmodulin-Binding Proteins
  • Cattle
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Activation
  • Kinetics
  • Magnesium / physiology
  • Phosphoprotein Phosphatases / metabolism*
  • Phosphorylation

Substances

  • Calmodulin
  • Calmodulin-Binding Proteins
  • Phosphoprotein Phosphatases
  • Magnesium
  • Calcium