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An inhibitor affinity chromatography (IAC) method has been developed for the analysis of inhibitor-protein interactions as a complementary approach to two-dimensional electrophoresis for functional proteomics studies. The procedure was developed utilizing a cyclin-dependent kinase 2 (Cdk2) inhibitor coupled to a polymeric resin and validated using a number of proteins interacting with the inhibitor with different specificities. Cdk2 and the other kinases bound and eluted from the resin in accordance with the relative in vitro potency of the inhibitor for each enzyme. Molecular interactions with the Cdk2 inhibitor were compared for HCT116 cancer cells versus rat pancreatic acinar cells. Proteins interacting with the ligand on the IAC matrix were identified by mass spectrometry. Isothermal calorimetry was used to confirm and quantitatively evaluate the binding affinity of some of the interacting proteins. Heat-shock protein (Hsp) 70 and Hsp27 were the strongest interactors with the inhibitor, displaying binding affinities comparable to those of Cdk2. These results support the use of IAC as a general method for the rapid identification and qualitative evaluation of the in vivo targets and potential side effects of a given drug.

Original publication

DOI

10.1002/pmic.200300431

Type

Journal article

Journal

Proteomics

Publication Date

07/2003

Volume

3

Pages

1287 - 1298

Keywords

Animals, Blotting, Western, CDC2-CDC28 Kinases, Calorimetry, Cell Line, Cell Line, Tumor, Chromatography, Cyclin A, Cyclin-Dependent Kinase 2, Dose-Response Relationship, Drug, Electrophoresis, Gel, Two-Dimensional, Electrophoresis, Polyacrylamide Gel, HSP27 Heat-Shock Proteins, HSP70 Heat-Shock Proteins, Heat-Shock Proteins, Humans, Insecta, Ligands, Mass Spectrometry, Models, Chemical, Neoplasm Proteins, Polymers, Protein Binding, Proteome, Rats, Spectrometry, Fluorescence, Thermodynamics, Trypsin