Jiang S T, Wang J H, Chang T, Chen C S
Department of Marine Food Science, National Taiwan Ocean University, Keelung, Taiwan, Republic of China.
Anal Biochem. 1997 Jan 15;244(2):233-38. doi: 10.1006/abio.1996.9872.
A simplified methodology for assaying the caseinolysis by calpains was developed. This methodology, including the incubation of calpain with casein and direct measurement of the absorbance at 500 nm, is based on the turbidity of the reaction mixture caused by the aggregation of hydrolysates during the reaction. Unlike the typical caseinolysis assay, this novel assay does not need to separate the substrate from hydrolysates and can be continuously monitored in visible wavelength range. The activity of calpain is expressed by the maximum reaction velocity (delta A500/min) at 25 degrees C).
开发了一种用于检测钙蛋白酶对酪蛋白水解作用的简化方法。该方法包括将钙蛋白酶与酪蛋白一起孵育,并直接测量500nm处的吸光度,其基于反应过程中水解产物聚集导致的反应混合物浊度。与典型的酪蛋白水解检测方法不同,这种新方法不需要将底物与水解产物分离,并且可以在可见波长范围内进行连续监测。钙蛋白酶的活性用25℃时的最大反应速度(ΔA500/分钟)表示。