Substrate optimization for monitoring cathepsin C activity in live cells

Bioorg Med Chem. 2009 Feb 1;17(3):1064-70. doi: 10.1016/j.bmc.2008.02.002. Epub 2008 Feb 7.

Abstract

A series of peptidic fluorogenic substrates were synthesized to develop a flow cytometry assay (FACS) to monitor the proteolytic activity of cathepsin C in live cells. Of the 16 substrates tested, (NH(2)-aminobutyric-homophenylalanine)(2)-rhodamine demonstrated the best reactivity and selectivity profile in the FACS assay using the B721 human B-lymphoblastoid cell line. The resulting FACS assay was validated through correlation of the IC(50) values with a competitive radiolabeling assay against a series of small molecule inhibitors of cathepsin C.

MeSH terms

  • Cathepsin C / antagonists & inhibitors
  • Cathepsin C / metabolism*
  • Cell Line, Tumor
  • Flow Cytometry
  • Fluorescent Dyes / chemistry*
  • Humans
  • Inhibitory Concentration 50
  • Isotope Labeling
  • Radioisotopes / chemistry
  • Rhodamines / chemical synthesis
  • Rhodamines / chemistry*
  • Substrate Specificity

Substances

  • Fluorescent Dyes
  • Radioisotopes
  • Rhodamines
  • Cathepsin C