Kuenzel E A, Krebs E G
Proc Natl Acad Sci U S A. 1985 Feb;82(3):737-41. doi: 10.1073/pnas.82.3.737.
A synthetic peptide having the sequence Arg-Arg-Arg-Glu-Glu-Thr-Glu-Glu-Glu was found to serve as a convenient substrate for the protein kinase generally referred to as casein kinase II. The enzyme exhibited an apparent Km of 500 microM for the peptide, as compared to an apparent Km of 50 microM for casein. The maximum velocities for phosphorylation of the peptide and of casein were similar. The peptide was not phosphorylated by any of eight other protein kinases, all of which were shown to be active toward their known substrates. The peptide was used to monitor activity during steps in the purification of casein kinase II from bovine liver. These experiments demonstrated that with this peptide it is now possible to obtain specific measurements of casein kinase II activity in crude enzyme preparations.
发现一种具有精氨酸 - 精氨酸 - 精氨酸 - 谷氨酸 - 谷氨酸 - 苏氨酸 - 谷氨酸 - 谷氨酸 - 谷氨酸序列的合成肽,可作为通常被称为酪蛋白激酶II的蛋白激酶的便捷底物。与酪蛋白的表观Km值50微摩尔相比,该酶对该肽的表观Km值为500微摩尔。该肽和酪蛋白磷酸化的最大速度相似。该肽不会被其他八种蛋白激酶中的任何一种磷酸化,所有这些蛋白激酶都显示对其已知底物有活性。该肽用于监测从牛肝中纯化酪蛋白激酶II过程中各步骤的活性。这些实验表明,使用这种肽现在可以在粗酶制剂中获得酪蛋白激酶II活性的特异性测量值。