Human plasma carboxypeptidase N. Isolation and characterization

J Biol Chem. 1978 Jun 10;253(11):3907-12.

Abstract

Human plasma carboxypeptidase N has been purified 2,600-fold from pooled, outdated plasma in a 30% yield. Isolation was accomplished by chromatography on DEAE-cellulose and on a p-aminobenzoyl-L-arginine-Sepharose 6B affinity column. Carbohydrate accounts for 17% of the weight calculated from its amino acid and carbohydrate composition. The enzyme appears to consist of three subunits of Mr = 83,000, 55,000, and 49,000 and contains a significant amount of bound zinc. Purified enzyme preparations are very sensitive to proteolytic degradation but are stable for at least 3 months at 4 degrees.

Publication types

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

MeSH terms

  • Amino Acids / analysis
  • Carboxypeptidases / blood*
  • Chromatography, Affinity
  • Chromatography, DEAE-Cellulose
  • Drug Stability
  • Fibrinolysin
  • Humans
  • Lysine Carboxypeptidase / blood*
  • Lysine Carboxypeptidase / isolation & purification
  • Methods
  • Trypsin
  • Zinc / analysis

Substances

  • Amino Acids
  • Carboxypeptidases
  • Lysine Carboxypeptidase
  • Trypsin
  • Fibrinolysin
  • Zinc