Conversion of protein kinase C from a Ca2+-dependent to an independent form of phorbol ester-binding protein by digestion with trypsin

Biochem Biophys Res Commun. 1986 Aug 29;139(1):320-6. doi: 10.1016/s0006-291x(86)80116-4.

Abstract

Tryptic fragments of protein kinase C containing the kinase (45 KDa) and phorbol ester-binding activity (38 KDa) were separated by Mono O column chromatography. The purified phorbol ester-binding fragment exhibits a higher affinity for phosphatidylserine than the native enzyme but comparable Kd for [3H]phorbol 12,13-dibutyrate as the native enzyme. This proteolytic fragment binds phorbol ester equally efficient either in the presence or absence of Ca2+ and the addition of the kinase fragment did not restore the Ca2+-requirement for the binding. These results indicate that protein kinase C is composed of two functionally distinct units which can be expressed independently after limited proteolysis with trypsin.

MeSH terms

  • Animals
  • Caenorhabditis elegans Proteins*
  • Calcium / pharmacology*
  • Carrier Proteins
  • Phorbol 12,13-Dibutyrate
  • Phorbol Esters / metabolism
  • Phosphatidylserines / pharmacology
  • Protein Kinase C / analysis*
  • Protein Kinases / analysis*
  • Rats
  • Receptors, Drug*
  • Receptors, Immunologic / analysis*
  • Tritium
  • Trypsin / pharmacology*

Substances

  • Caenorhabditis elegans Proteins
  • Carrier Proteins
  • Phorbol Esters
  • Phosphatidylserines
  • Receptors, Drug
  • Receptors, Immunologic
  • phorbol ester binding protein
  • phorbol ester receptor
  • Tritium
  • Phorbol 12,13-Dibutyrate
  • Protein Kinases
  • Protein Kinase C
  • Trypsin
  • Calcium