Purification and characterization of an endogenous inhibitor specific to the Z-Leu-Leu-Leu-MCA degrading activity in proteasome and its identification as heat-shock protein 90

FEBS Lett. 1994 May 16;344(2-3):229-33. doi: 10.1016/0014-5793(94)00388-2.

Abstract

We previously identified a benzyloxycarbonyl(Z)-Leu-Leu-Leu-4-methylcoumaryl-7-amide (ZLLL-MCA) degrading activity in proteasome as a candidate for the regulator of neurite outgrowth. As its counterpart, we purified a protein from bovine brain that specifically inhibits the ZLLL-MCA degrading activity in proteasome. This protein is heat stable and has no effect on the other catalytic activities in proteasome, or on the activities of trypsin, chymotrypsin, or m- and mu-calpains either. The molar ratio of inhibitor-to-proteasome that inhibits 50% of the ZLLL-MCA degrading activity of proteasome is 1:1. The inhibitory mechanism of the inhibitor against proteasome is non-competitive. Finally, the inhibitor was identified as heat-shock protein 90 (HSP90) by partial amino acid sequencing and immunodetection. The results suggest that HSP90 initiates neurite outgrowth through the inhibition of the ZLLL-MCA degrading activity in proteasome.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain / enzymology
  • Cattle
  • Electrophoresis, Polyacrylamide Gel
  • Endopeptidases / metabolism*
  • Fluorescent Dyes
  • Heat-Shock Proteins / chemistry
  • Heat-Shock Proteins / isolation & purification*
  • Molecular Sequence Data
  • Molecular Weight
  • Oligopeptides / metabolism*
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / isolation & purification*
  • Protease Inhibitors / pharmacology
  • Sequence Analysis

Substances

  • Fluorescent Dyes
  • Heat-Shock Proteins
  • Oligopeptides
  • Protease Inhibitors
  • benzyloxycarbonylleucyl-leucyl-leucyl-4-methyl-coumaryl-7-amide
  • Endopeptidases