A liquid chromatography/mass spectrometry-based method for the selection of ATP competitive kinase inhibitors

J Biomol Screen. 2005 Aug;10(5):447-55. doi: 10.1177/1087057105274846.

Abstract

The currently approved kinase inhibitors for therapeutic uses and a number of kinase inhibitors that are undergoing clinical trials are directed toward the adenosine triphosphate (ATP) binding site of protein kinases. The 5'-fluorosulfonylbenzoyl 5'-adenosine (FSBA) is an ATP-affinity reagent that covalently modifies a conserved lysine present in the nucleotide-binding site of most kinases. The authors have developed a liquid chromatography/mass spectrometry-based method to monitor binding of ATP competitive protein kinase inhibitors using FSBA as a nonselective activity-based probe for protein kinases. Their method provides a general, rapid, and reproducible means to screen and validate selective ATP competitive inhibitors of protein kinases.

MeSH terms

  • Adenosine / analogs & derivatives
  • Adenosine / pharmacology
  • Adenosine Triphosphate / chemistry
  • Affinity Labels / pharmacology
  • Apoptosis
  • Autoradiography
  • Binding Sites
  • Binding, Competitive
  • CDC2-CDC28 Kinases / metabolism
  • Cell Differentiation
  • Chromatography, Liquid / methods*
  • Cyclin-Dependent Kinase 2
  • Drug Evaluation, Preclinical / methods*
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Inhibitors / pharmacology*
  • Mass Spectrometry / methods*
  • Models, Chemical
  • Phosphotransferases / metabolism
  • Signal Transduction
  • Time Factors

Substances

  • Affinity Labels
  • Enzyme Inhibitors
  • 5'-(4-fluorosulfonylbenzoyl)adenosine
  • Adenosine Triphosphate
  • Phosphotransferases
  • CDC2-CDC28 Kinases
  • Cyclin-Dependent Kinase 2
  • Adenosine