Proteome profiling reveals potential cellular targets of staurosporine using a clickable cell-permeable probe

Chem Commun (Camb). 2011 Oct 28;47(40):11306-8. doi: 10.1039/c1cc14824a. Epub 2011 Sep 16.

Abstract

A clickable, affinity-based probe (AfBP), which was modified from staurosporine (a natural product kinase inhibitor), has been synthesized and used in situ for activity-based proteome profiling of potential cellular targets of staurosporine in HepG2 cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Click Chemistry*
  • Hep G2 Cells
  • Humans
  • Molecular Probes / chemical synthesis
  • Molecular Probes / chemistry*
  • Molecular Probes / metabolism*
  • Permeability
  • Protein Kinase Inhibitors / metabolism*
  • Protein Kinases / metabolism
  • Proteomics / methods*
  • Staurosporine / metabolism*

Substances

  • Molecular Probes
  • Protein Kinase Inhibitors
  • Protein Kinases
  • Staurosporine