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Updated: Jul 5, 2026

A Convenient and General Expression Platform for the Production of Secreted Proteins from Human Cells
Published on: July 31, 2012
Bacterial expression and purification of interleukin-2 tyrosine kinase: single step separation of the chaperonin
Raji E Joseph1, Amy H Andreotti
1Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, 4208 MBB, Ames, IA 50011, USA.
Abstract:
Biochemical and biophysical characterization of kinases requires large quantities of purified protein. Here, we report the bacterial expression and purification of active Itk kinase domain (a Tec family kinase) using ArcticExpress cells that co-express the chaperonin system Cpn60/10 from Oleispira antarctica. We describe a simple one step MgCl2/ATP/KCl incubation procedure to remove the co-purifying chaperonin impurity. Chaperonin co-purification is a common problem encountered during protein purification and the simple incubation step described here completely overcomes this problem. The approach targets the chaperonin system rather than the protein of interest and is therefore widely applicable to other protein targets.

