Comparison of extracellular matrix-degrading activities between 64-kDa and 90-kDa gelatinases purified in inhibitor-free forms from human schwannoma cells

J Biochem. 1992 Jan;111(1):74-80. doi: 10.1093/oxfordjournals.jbchem.a123721.

Abstract

Two kinds of gelatinases (or type IV collagenases), 90-kDa and 64-kDa gelatinases, were purified in a tissue inhibitor of metalloproteinases (TIMP)- or TIMP-2-free form from the serum-free conditioned medium of human schwannoma YST-3 cells, and their activities on extracellular matrix proteins were compared. Sequential chromatographies on a gelatin-Sepharose column, an LCA-agarose column, and a gel filtration column in the presence of 5 M urea yielded 600 micrograms of the 64-kDa enzyme and 45 micrograms of the 90-kDa enzyme from 2.8 liters of the conditioned medium. The purified enzymes showed high gelatinolytic activities without activation by p-aminophenyl mercuric acetate (APMA), indicating that 5 M urea used in the final chromatography not only dissociated the inhibitors from the progelatinases but also activated the proenzymes. The inhibitor-free gelatinases showed a much higher activity than the APMA-activated inhibitor-bound enzymes. The specific activity of the 90-kDa enzyme was nearly 25 times higher than that of the 64-kDa enzyme. The 90-kDa gelatinase hydrolyzed type I collagen as well as native and pepsin-treated type IV collagens at 30 degrees C, while at 37 degrees C it potently hydrolyzed types I, III, and IV collagens but not fibronectin or laminin. The 64-kDa gelatinase showed a similar substrate specificity to that of the 90-kDa enzyme, except that it did not hydrolyze type I collagen and native type IV collagen at 30 degrees C.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Collagen / metabolism*
  • Extracellular Matrix Proteins / metabolism*
  • Fibronectins / metabolism
  • Humans
  • Immunoblotting
  • Laminin / metabolism
  • Matrix Metalloproteinase 9
  • Microbial Collagenase / chemistry
  • Microbial Collagenase / isolation & purification
  • Microbial Collagenase / metabolism*
  • Molecular Weight
  • Neurilemmoma
  • Phenylmercuric Acetate / analogs & derivatives
  • Phenylmercuric Acetate / pharmacology
  • Protease Inhibitors / pharmacology
  • Substrate Specificity
  • Tumor Cells, Cultured

Substances

  • Extracellular Matrix Proteins
  • Fibronectins
  • Laminin
  • Protease Inhibitors
  • 4-aminophenylmercuriacetate
  • Collagen
  • Microbial Collagenase
  • Matrix Metalloproteinase 9
  • Phenylmercuric Acetate