Subcellular localization, partial purification, and characterization of a dynorphin processing endopeptidase from bovine pituitary

J Neurochem. 1991 Jan;56(1):320-9. doi: 10.1111/j.1471-4159.1991.tb02598.x.

Abstract

An enzyme capable of cleaving dynorphin B-29 to dynorphin B-13 is present in bovine pituitary, with 40- to 50-fold higher specific activity in the posterior and intermediate lobes than in the anterior lobe. Subcellular fractionation of bovine neurointermediate pituitary shows that this enzyme is present in the peptide-containing secretory vesicles. The enzyme has been purified 2,800-fold from whole bovine pituitaries using ion-exchange and gel filtration chromatography. Purified dynorphin-converting enzyme has a neutral pH optimum, and is subsantially inhibited by the thiol-protease inhibitor p-chloromercuriphenylsulfonic acid, but not by serine or metalloprotease inhibitors. The purified enzyme processes dynorphin B-29 at Arg14, producing both dynorphin B-14 and dynorphin B-13 in a 5:1 ratio. No other cleavages are observed, suggesting that the activity is free from other proteases and is specific for single Arg sequences. Purified enzyme also processes dynorphin A-17 at the single Arg cleavage site, generating both dynorphin A-8 and A-9 in a 7:1 ratio. The tissue distribution, subcellular localization, and substrate specificity of this enzyme are consistent with a physiological role in the processing of dynorphin B-29 and dynorphin A-17, and possibly other peptides, at single Arg residues.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 4-Chloromercuribenzenesulfonate
  • Amino Acid Sequence
  • Animals
  • Cattle
  • Cell Fractionation
  • Centrifugation, Density Gradient
  • Chromatography
  • Chromatography, High Pressure Liquid
  • Dynorphins / metabolism*
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Pituitary Gland / enzymology*
  • Pituitary Gland / ultrastructure
  • Serine Endopeptidases / isolation & purification
  • Serine Endopeptidases / metabolism*
  • Serine Proteinase Inhibitors
  • Substrate Specificity
  • Tissue Distribution

Substances

  • Serine Proteinase Inhibitors
  • 4-Chloromercuribenzenesulfonate
  • Dynorphins
  • Serine Endopeptidases
  • dynorphin-converting endopeptidase