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Chem Biol. 2004 Feb;11(2):211-23.

A three-hybrid approach to scanning the proteome for targets of small molecule kinase inhibitors.

Author information

1
GPC Biotech AG, 20 Fraunhoferstrasse, Planegg/Martinsried 82152, Germany.

Abstract

In this study, we explored the application of a yeast three-hybrid (Y3H)-based compound/protein display system to scanning the proteome for targets of kinase inhibitors. Various known cyclin-dependent kinase (CDK) inhibitors, including purine and indenopyrazole analogs, were displayed in the form of methotrexate-based hybrid ligands and deployed in cDNA library or yeast cell array-based screening formats. For all inhibitors, known cell cycle CDKs as well as novel candidate CDK-like and/or CDK-unrelated kinase targets could be identified, many of which were independently confirmed using secondary enzyme assays and affinity chromatography. The Y3H system described here may prove generally useful in the discovery of candidate drug targets.

PMID:
15123283
DOI:
10.1016/j.chembiol.2004.02.001
[Indexed for MEDLINE]
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