Purification of the catalytic subunit of protein phosphatase-1 from Drosophila melanogaster

Biochem Biophys Res Commun. 1987 May 14;144(3):1175-81. doi: 10.1016/0006-291x(87)91435-5.

Abstract

The catalytic subunit of phosphatase-1 has been purified from Drosophila melanogaster by precipitation with (NH4)2SO4 and ethanol, by affinity chromatography on heparin-Sepharose and by fast protein liquid chromatography on Mono Q beads. The preparation is homogeneous as tested by SDS gel electrophoresis and has a molecular mass of 33,000. The phosphatase specifically dephosphorylates the beta subunit of phosphorylase kinase. Its phosphorylase phosphatase activity is inhibited by inhibitor-1, inhibitor-2, protamine and histone H2B while is stimulated by histone H1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drosophila melanogaster / enzymology*
  • Kinetics
  • Macromolecular Substances
  • Molecular Weight
  • Phosphoprotein Phosphatases / isolation & purification*
  • Phosphoprotein Phosphatases / metabolism
  • Protein Phosphatase 1
  • Substrate Specificity

Substances

  • Macromolecular Substances
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 1