Ahmed K, Wilson M J, Davis A T
Biochim Biophys Acta. 1975 Jan 23;377(1):80-3. doi: 10.1016/0005-2744(75)90288-0.
The maximal rates of the protein kinase (ATP: protein phosphotransferase, EC 2.7.1.37) reaction studied with chicken egg yolk phosvitin as substrate are dependent on the level of dephosphorylation of phosvitin. 30 per cent dephospho-phosvitin gives the optimal initial rates. With varying levels of dephosphorylation, the apparent Km for the substrate also changes in a biphasic manner. If this factor is taken into account, and a suitable adjustment is made for the concentration of dephospho-phosvitin in the reaction it is possible to achieve maximal rates for the kinase reaction with phosvitin preparations of varying levels of dephosphorylation. Such a consideration is important for comparing the results of protein kinase studies using phosvitin as the substrate.
以鸡卵黄磷蛋白为底物研究的蛋白激酶(ATP:蛋白磷酸转移酶,EC 2.7.1.37)反应的最大速率取决于磷蛋白的去磷酸化水平。30%的去磷酸化磷蛋白可给出最佳初始速率。随着去磷酸化水平的变化,底物的表观Km也呈双相变化。如果考虑到这一因素,并对反应中去磷酸化磷蛋白的浓度进行适当调整,就有可能使不同去磷酸化水平的磷蛋白制剂的激酶反应达到最大速率。这种考虑对于比较以磷蛋白为底物的蛋白激酶研究结果很重要。