Mentel Mihaela, Badea Rodica A, Necula-Petrareanu Georgiana, Mallikarjuna Sujay T, Ionescu Aura E, Szedlacsek Stefan E
Department of Enzymology, Institute of Biochemistry of the Romanian Academy, Splaiul Independentei 296, 060031, Bucharest 17, Romania.
Methods Mol Biol. 2016;1447:39-66. doi: 10.1007/978-1-4939-3746-2_3.
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.
蛋白酪氨酸磷酸酶(PTP)是一大类酶,它们与蛋白酪氨酸激酶共同作用,控制蛋白质的酪氨酸磷酸化,从而在细胞信号传导中发挥主要作用。在此,我们提供了详细的方案,用于表达和纯化RPTPμ的催化结构域、全长Eya3以及PTPBR7的细胞外区域。还描述了评估由此获得的重组蛋白纯度的方法。对于纯化的Eya3磷酸酶,我们提供了使用显色、荧光或肽底物进行酶活性测定的方案。还描述了通过不同的图形和基于计算机的程序测定动力学参数的方法。