Brain cathepsin B cleaves a caspase substrate

Biochemistry (Mosc). 2008 Mar;73(3):332-6. doi: 10.1134/s0006297908030140.

Abstract

We show that an enzyme exists in rat brain capable of cleaving the caspase-3 specific peptide substrate Ac-DEVD-AMC at low pH. The enzyme shows properties of a cysteine protease and is localized, predominantly, in lysosomes. We have purified this enzyme from rat brain and identified it by MALDI-TOF MS. The enzyme possessing "acidic" DEVDase activity in rat brain appears to be cathepsin B. It remains obscure, whether cathepsin B participates in cleavage of caspase-3 substrates in vivo. We suggest that under certain conditions (e.g. in hypoxia) cathepsin B participates in cleavage of caspase-3 substrates in brain cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / enzymology*
  • Caspase 3 / metabolism*
  • Cathepsin B / isolation & purification
  • Cathepsin B / metabolism*
  • Coumarins / metabolism
  • Cysteine Proteinase Inhibitors / metabolism
  • Cysteine Proteinase Inhibitors / pharmacology
  • Hydrogen-Ion Concentration
  • Oligopeptides / metabolism
  • Rats
  • Sulfhydryl Reagents / pharmacology

Substances

  • Ac-aspartyl-glutamyl-valyl-aspartyl-aminomethylcoumarin
  • Coumarins
  • Cysteine Proteinase Inhibitors
  • Oligopeptides
  • Sulfhydryl Reagents
  • Caspase 3
  • Cathepsin B