Purification and characterization of phosphatidylinositol 4-phosphate 5-kinases

Biochem J. 1992 Dec 1;288 ( Pt 2)(Pt 2):637-42. doi: 10.1042/bj2880637.

Abstract

We detail the purification and characterization of three distinct isoforms of PtdIns4P 5-kinase present in bovine brain. One of these, PtdIns4P 5-kinase C, was purified to apparent homogeneity, and SDS/PAGE analysis demonstrated a single polypeptide and molecular mass 53 KDa. These three isoforms were shown to differ in their kinetic properties, and immunological characterization with an antibody raised to PtdIns4P 5-kinase C demonstrated that this isoform was unrelated to the other two. Furthermore, PtdIns4P 5-kinase C was shown to be the bovine brain homologue of the Type II PtdIns4P 5-kinase previously purified from human erythrocytes [Bazenet, Ruano, Brockman & Anderson (1990) J. Biol. Chem. 265, 18012-18022].

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / enzymology
  • Cattle
  • Cross Reactions
  • Cytosol / enzymology
  • Erythrocytes / immunology
  • Humans
  • Isoenzymes / immunology
  • Isoenzymes / isolation & purification
  • Kinetics
  • Phosphatidylinositol Phosphates*
  • Phosphatidylinositols / metabolism
  • Phosphotransferases (Alcohol Group Acceptor)*
  • Phosphotransferases / immunology
  • Phosphotransferases / isolation & purification*
  • Substrate Specificity

Substances

  • Isoenzymes
  • Phosphatidylinositol Phosphates
  • Phosphatidylinositols
  • phosphatidylinositol 4-phosphate
  • Phosphotransferases
  • Phosphotransferases (Alcohol Group Acceptor)
  • 1-phosphatidylinositol-4-phosphate 5-kinase