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Updated: Mar 16, 2026

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
Published on: June 30, 2019
Expression, Purification, and Kinetic Analysis of PTP Domains
Mihaela Mentel1, Rodica A Badea1, Georgiana Necula-Petrareanu1
1Department of Enzymology, Institute of Biochemistry of the Romanian Academy, Splaiul Independentei 296, 060031, Bucharest 17, Romania.
Abstract:
Protein tyrosine phosphatases (PTP) are a large group of enzymes which work together with protein tyrosine kinases to control the tyrosine phosphorylation of proteins, thus playing a major role in cellular signaling. Here, we provide detailed protocols for expression and purification of the catalytic domain of RPTPμ and full length Eya3 as well as the extracellular region of PTPBR7. Methods are described for evaluation of the purity of the recombinant proteins thus obtained. For the purified Eya3 phosphatase we provide protocols for enzyme activity assay using either chromogenic, fluorescent, or peptide substrates. Determination of kinetic parameters by different graphical and computer-based procedures is also described.
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