Action of neurohypophysial granule Lys-Arg endopeptidase on synthetic polypeptides comprising the processing sequence of provasopressin-neurophysin

Biosci Rep. 1994 Aug;14(4):171-8. doi: 10.1007/BF01200246.

Abstract

Neurohypophysial granule Ca(2+)-dependent endopeptidases have been allowed to act on synthetic polypeptides derived from the N-terminal sequence of bovine provasopressin-neurophysin, namely vasopressinyl-glycyl-lysyl-arginyl-alanylamide and vasopressinyl-glycyl-lysyl-arginyl-alanyl-methionyl-serinamide+ ++. Membrane-bound enzymes have been used at pH 5.5 for 16 hr at 37 degrees C. Products have been identified by high-pressure liquid chromatography (HPLC) and by mass spectrometry performed on substances isolated by HPLC. With both substrates, vasopressinyl-Gly-Lys-Arg(OH) has been identified as a product confirming the Lys-Arg specificity previously observed on small peptide fluorogenic substrates. Cleavage yields, however, appear low suggesting that some factors are missing, for example a targeting action of the precursor neurophysin domain to the granule membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Arginine
  • Arginine Vasopressin / metabolism*
  • Cattle
  • Cytoplasmic Granules / enzymology
  • Endopeptidases / metabolism*
  • Hydrogen-Ion Concentration
  • Hydrolysis
  • In Vitro Techniques
  • Lysine
  • Molecular Sequence Data
  • Neurophysins / metabolism*
  • Oxytocin*
  • Peptide Fragments / chemical synthesis
  • Peptide Fragments / metabolism
  • Pituitary Gland, Posterior / enzymology*
  • Protein Precursors / metabolism*
  • Rats
  • Vasopressins / metabolism*

Substances

  • Neurophysins
  • Peptide Fragments
  • Protein Precursors
  • Vasopressins
  • Arginine Vasopressin
  • Oxytocin
  • Arginine
  • Endopeptidases
  • Lysine