Henderson P J
Biochem J. 1973 Sep;135(1):101-7. doi: 10.1042/bj1350101.
A statistical treatment of steady-state enzyme kinetic measurements is described that allows for depletion of free substrate or free inhibitor concentrations owing to significant binding to the enzyme. V(max.), K(m) or K(i), enzyme concentration, the concentration of substrate or inhibitor required for a half-maximal effect and standard errors of these parameters can be calculated from dose-response measurements; the concentration of each component of the system may be estimated also. The statistically best values of the parameters are used to convert dose-response curves into convenient linear forms. The method is applied to dose-response measurements of hydroxyquinoline N-oxide inhibition of bacterial respiration and aminopterin inhibition of dihydrofolate reductase. Two FORTRAN programs for this method have been deposited as Supplementary Publication no. SUP 50019 at the National Lending Library for Science and Technology, Boston Spa, Yorks. LS23 7BQ, U.K., from whom copies may be obtained on the terms indicated in Biochem. J. (1973) 131, 5.
本文描述了一种对稳态酶动力学测量的统计学处理方法,该方法考虑到由于与酶的显著结合导致游离底物或游离抑制剂浓度的消耗。可以从剂量 - 反应测量中计算出V(max.)、K(m)或K(i)、酶浓度、产生半最大效应所需的底物或抑制剂浓度以及这些参数的标准误差;系统中各组分的浓度也可以估算。参数的统计学最佳值用于将剂量 - 反应曲线转换为方便的线性形式。该方法应用于羟基喹啉N - 氧化物对细菌呼吸的抑制以及氨基蝶呤对二氢叶酸还原酶的抑制的剂量 - 反应测量。关于此方法的两个FORTRAN程序已作为补充出版物SUP 50019存放在英国约克郡波士顿温泉市国家科技出借图书馆,邮编LS23 7BQ,可按《生物化学杂志》(1973) 131, 5中所示条款从该处获取副本。