King M J, Sale G J
Department of Biochemistry, School of Biochemical and Physiological Sciences, University of Southampton, England.
FEBS Lett. 1988 Sep 12;237(1-2):137-40. doi: 10.1016/0014-5793(88)80187-x.
Synthetic peptide 1142-1153 of the insulin receptor was phosphorylated on tyrosine by the insulin receptor and found to be a potent substrate for dephosphorylation by rat liver particulate and soluble phosphotyrosyl protein phosphatases. Apparent Km values were approximately 5 microM. Vm values (nmol phosphate removed/min per mg protein) were 0.62 (particulate) and 0.2 (soluble). This corresponds to 80% of total activity being membrane-associated, indicating that membrane-bound phosphatases are important receptor phosphatases. The phosphatase activities were distinct from acid and alkaline phosphatase. In conclusion peptide 1142-1153 provides a useful tool for the further study and characterization of phosphotyrosyl protein phosphatases.
胰岛素受体的合成肽1142 - 1153被胰岛素受体磷酸化于酪氨酸上,并被发现是大鼠肝脏微粒体和可溶性磷酸酪氨酸蛋白磷酸酶去磷酸化的有效底物。表观Km值约为5微摩尔。Vm值(每毫克蛋白质每分钟去除的磷酸盐纳米摩尔数)分别为0.62(微粒体)和0.2(可溶性)。这相当于总活性的80%与膜相关,表明膜结合磷酸酶是重要的受体磷酸酶。磷酸酶活性与酸性和碱性磷酸酶不同。总之,肽1142 - 1153为进一步研究和表征磷酸酪氨酸蛋白磷酸酶提供了一个有用的工具。