Nieto M A, Palacián E
Biochim Biophys Acta. 1983 Dec 12;749(2):204-10. doi: 10.1016/0167-4838(83)90254-6.
The reagents citraconic and dimethylmaleic anhydrides modify the amino groups of proteins in a reversible way, the modified amino groups being regenerated at moderate acid pH. To use these reagents efficiently it is important to know the stabilities of the modifed groups under different experimental conditions. We have studied the kinetics of deacylation of ovalbumin amino groups modified with citraconic and dimethylmaleic anhydrides, under different conditions of temperature (0-40 degrees C) and pH (4-8). The deacylation of the modified groups follows pseudo-first-order kinetics under all experimental conditions studied. For both reagents, the dependence of the rate of deacylation on temperature obeys the Arrhenius equation, and the logarithm of the apparent deacylation constant shows a linear dependence on pH. From the experimental data, equations have been obtained for both reagents relating the deacylation constant with temperature and pH. These equations allow the calculation of the deacylation constant and the half-life of the modified groups for any conditions of temperature and pH within the experimental intervals studied.
柠康酸酐和二甲基马来酸酐试剂能以可逆方式修饰蛋白质的氨基,修饰后的氨基在适度酸性pH条件下会再生。为了有效使用这些试剂,了解修饰基团在不同实验条件下的稳定性很重要。我们研究了在不同温度(0 - 40摄氏度)和pH(4 - 8)条件下,用柠康酸酐和二甲基马来酸酐修饰的卵清蛋白氨基的脱酰化动力学。在所研究的所有实验条件下,修饰基团的脱酰化遵循准一级动力学。对于这两种试剂,脱酰化速率对温度的依赖性符合阿仑尼乌斯方程,表观脱酰化常数的对数对pH呈线性依赖关系。根据实验数据,已得到两种试剂的脱酰化常数与温度和pH相关的方程。这些方程可用于计算在所研究的实验区间内任何温度和pH条件下修饰基团的脱酰化常数和半衰期。