Application of poly-L-lysine to purification of leukocyte cathepsin G by affinity chromatography

Chem Pharm Bull (Tokyo). 1992 Jun;40(6):1634-6. doi: 10.1248/cpb.40.1634.

Abstract

Poly-L-lysine with molecular masses of 3.3-290 kDa increased the amidolytic activities of leukocyte elastase and cathepsin G at low concentration, but had little effect on the activities of pancreatic elastase, alpha-chymotrypsin, plasmin and thrombin. Highly purified cathepsin G was obtained from column of EAH Sepharose 4B or Suc-L-Tyr-D-Leu-D-Val-pNA-Sepharose (affinity chromatography) by elution with poly-L-lysine solution (0.4 mg/ml, molecular weight (MW.) 290000 or 2.2 mg/ml, MW. 3300). Leukocyte elastase, adsorbed to Suc-L-Tyr-D-Leu-D-Val-pNA-Sepharose, was not eluted with poly-L-lysine solution. The amino acid composition of purified cathepsin G has been determined.

MeSH terms

  • Amino Acid Sequence
  • Cathepsin G
  • Cathepsins / blood
  • Cathepsins / isolation & purification*
  • Chromatography, Affinity
  • Humans
  • In Vitro Techniques
  • Leukocytes / chemistry*
  • Molecular Sequence Data
  • Polylysine / pharmacology*
  • Serine Endopeptidases

Substances

  • Polylysine
  • Cathepsins
  • Serine Endopeptidases
  • CTSG protein, human
  • Cathepsin G