A synthetic peptide substrate for selective assay of protein kinase C

Biochem Biophys Res Commun. 1990 Feb 14;166(3):1220-7. doi: 10.1016/0006-291x(90)90996-z.

Abstract

Among various phosphate acceptor proteins and peptides so far tested, a synthetic peptide having the sequence surrounding Ser(8) of myelin basic protein, Gln-Lys-Arg-Pro-Ser(8)-Gln-Arg-Ser-Lys-Tyr-Leu, (MBP4-14), is the most specific and convenient substrate which can be used for selective assay of protein kinase C. This peptide is not phosphorylated by cyclic AMP-dependent protein kinase, casein kinases I and II, Ca2+/calmodulin-dependent protein kinase II, or phosphorylase kinase, and can be routinely used for the assay of protein kinase C with low background in the crude tissue extracts. The Km value is considerably low (7 microM) with a Vmax value of twice as much as that for H1 histone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain / enzymology
  • Casein Kinases
  • Isoenzymes / metabolism
  • Kinetics
  • Lung / enzymology
  • Molecular Sequence Data
  • Muscles / enzymology
  • Myelin Basic Protein / chemical synthesis*
  • Oligopeptides / chemical synthesis*
  • Oligopeptides / metabolism
  • Protein Kinase C / metabolism*
  • Protein Kinases / metabolism
  • Rabbits
  • Rats
  • Substrate Specificity

Substances

  • Isoenzymes
  • Myelin Basic Protein
  • Oligopeptides
  • Protein Kinases
  • Casein Kinases
  • Protein Kinase C