Cathepsin B in human leukocytes

Clin Chem Lab Med. 1998 Sep;36(9):703-7. doi: 10.1515/CCLM.1998.124.

Abstract

We have applied a method using the fluorigenic substrate benzoloxycarbonyl-Arg-Arg-amido-4-methylcoumarin to measure cathepsin B, a thiol proteinase, in homogenates of human leukocytes. Data like pH optimum, stability, influence of thiol groups and effects of thiol proteinase inhibitors, lack of binding to Concanavalin A and lack of contribution to the fluorescence by other cathepsins indicate that cathepsin B is the enzyme measured. Although the activity of the enzyme was linear with respect to time at all protein concentrations measured, there was an acceptable 10% deviation of the enzyme activity from linearity as a function of protein concentration. The enzyme in the homogenate was stable at 0 degrees C but was rapidly inactivated at 50 degrees C and above pH 6.5-7. Very limited activation on the one hand and variable inhibition on the other was seen by reagents containing thiol groups and thiol proteinase inhibitors respectively. Latency (60% of the enzyme activity) indicates a probable subcellular lysosomal localization. There is no affinity towards the lectin Concanavalin A and the Km value was around 1 mmol/l. Normal enzyme activity values in leukocyte homogenates were determined.

MeSH terms

  • Adult
  • Cathepsin B / antagonists & inhibitors
  • Cathepsin B / blood*
  • Cysteine Proteinase Inhibitors / pharmacology
  • Enzyme Stability
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Leukocytes / enzymology*
  • Male
  • Serine Proteinase Inhibitors / pharmacology
  • Substrate Specificity

Substances

  • Cysteine Proteinase Inhibitors
  • Serine Proteinase Inhibitors
  • Cathepsin B