Ostoa-Saloma P, Ramírez J, Perez-Montfort R
Departamento de Microbiología, Universidad Nacional Autónoma de México, Mexico, D.F.
Anal Biochem. 1989 Feb 1;176(2):239-43. doi: 10.1016/0003-2697(89)90302-3.
A qualitative and quantitative method to assay proteolytic degradation of casein with a spectrofluorometer was developed. Proteolysis produced by different pure or mixed proteinases in a pH range 2 to 7.4 quenches the fluorescence emitted at a wavelength of 350 nm by casein excited at 300 nm in less than 5 min. This method is very sensitive, fast, and requires minimal sample preparation. Proteinases that do not generate peptides appropriate for fluorescence quenching cannot be detected with this assay and proteinases with intrinsic fluorescence may require special adjustments of the spectrofluorometer. This method monitors the disappearance of intact substrate proteins continuously, omitting the separation step necessary in other methods to measure product peptides.
开发了一种用荧光分光光度计测定酪蛋白蛋白水解降解的定性和定量方法。在pH值2至7.4范围内,不同的纯蛋白酶或混合蛋白酶产生的蛋白水解作用会在不到5分钟的时间内淬灭酪蛋白在300nm激发下在350nm波长处发射的荧光。该方法非常灵敏、快速,且所需样品制备最少。不能产生适合荧光淬灭的肽段的蛋白酶无法用该测定法检测到,而具有内在荧光的蛋白酶可能需要对荧光分光光度计进行特殊调整。该方法连续监测完整底物蛋白的消失,省去了其他测量产物肽段的方法中必需的分离步骤。