Characterization of dynorphin A-converting enzyme in human spinal cord. An endoprotease related to a distinct conversion pathway for the opioid heptadecapeptide?

J Biol Chem. 1992 Oct 25;267(30):21324-8.

Abstract

A highly specific proteinase, converting dynorphin A (1-17) to enkephalins, was isolated from the human spinal cord and subjected to further characterization. The enzyme was found to be a thiol-dependent protein with a relative molecular mass of 50 kDa and a pH optimum between 5.0 and 5.5. This proteinase appears to exclusively convert dynorphin A (1-17) to Leu-enkephalin and its COOH-terminal extensions Leu-enkephalin-Arg6 (which was a major conversion product) and Leu-enkephalin-Arg6-Arg7 but not the other prodynorphin- or proenkephalin-derived peptides. This high specificity toward a single structure is suggested to be involved in a distinct processing pathway associated with the generation of the opioid peptides with selectivity for delta-opioid receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Chromatography, Gel
  • Chromatography, High Pressure Liquid
  • Cysteine Endopeptidases / isolation & purification
  • Cysteine Endopeptidases / metabolism*
  • Dynorphins / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Enkephalins / metabolism
  • Humans
  • Molecular Sequence Data
  • Peptide Fragments / metabolism
  • Receptors, Opioid, delta / metabolism
  • Spinal Cord / enzymology*
  • Substrate Specificity

Substances

  • Enkephalins
  • Peptide Fragments
  • Receptors, Opioid, delta
  • Dynorphins
  • Cysteine Endopeptidases
  • dynorphin A-converting enzyme