Thompson V F, Saldaña S, Cong J, Goll D E
Muscle Biology Group, University of Arizona, Tucson, Arizona, 85721, USA.
Anal Biochem. 2000 Mar 15;279(2):170-8. doi: 10.1006/abio.1999.4475.
The use of 4,4-difluoro-5,7-dimethyl-4-bora-3a, 4a-diaza-s-indacene-3-propionic acid (BODIPY-FL) labeled casein in autoquenching assays of proteolytic activity has been recently described, and we have adapted this assay to measurement of calpain activity. BODIPY-FL coupled to casein at a ratio of 8 mol of BODIPY-FL/mol of casein or higher produces a BODIPY-FL-casein substrate that can be used in an autoquenching assay of calpain proteolytic activity. This assay has a number of advantages for measuring calpain activity. (1) The procedure does not require precipitation and removal of undegraded protein, so it is much faster than other procedures that require a precipitation step, and it can be used directly in kinetic assays of proteolytic activity. (2) The BODIPY-FL-casein assay is easily adapted to a microtiter plate format, so it can be used to screen large numbers of samples. (3) Casein is an inexpensive and readily available protein substrate that more closely mimics the natural substrates of endoproteinases, such as the calpains, than synthetic peptide substrates do. Casein has K(m) values for micro- and m-calpain that are similar to those of other substrates such as fodrin or MAP2 that may be "natural" substrates for the calpains, and there is no reason to believe that calpain hydrolysis of casein is inherently different from hydrolysis of fodrin or MAP2, which are much less accessible as substrates for protease assays. (4) The BODIPY-FL-casein assay is capable of detecting 10 ng ( approximately 5 nM) of calpain and is nearly as sensitive as the most sensitive calpain assay reported thus far. (5) The BODIPY-FL-casein assay is as reproducible as the FITC-casein assay, whose reproducibility is comparable to or better than the reproducibility of other methods used to assay calpain activity. The BODIPY-FL-casein assay is a general assay for proteolytic activity and can be used with any protease that cleaves casein.
最近已报道了在蛋白水解活性的自猝灭分析中使用4,4-二氟-5,7-二甲基-4-硼-3a,4a-二氮杂-s-茚满-3-丙酸(BODIPY-FL)标记的酪蛋白,并且我们已将该分析方法应用于钙蛋白酶活性的测定。以8摩尔BODIPY-FL/摩尔酪蛋白或更高的比例与酪蛋白偶联的BODIPY-FL可产生一种BODIPY-FL-酪蛋白底物,该底物可用于钙蛋白酶蛋白水解活性的自猝灭分析。该分析方法在测定钙蛋白酶活性方面具有许多优点。(1)该方法不需要沉淀和去除未降解的蛋白质,因此比其他需要沉淀步骤的方法快得多,并且可直接用于蛋白水解活性的动力学分析。(2)BODIPY-FL-酪蛋白分析很容易适用于微量滴定板形式,因此可用于筛选大量样品。(3)酪蛋白是一种廉价且容易获得的蛋白质底物,与合成肽底物相比,它更接近地模拟内肽酶(如钙蛋白酶)的天然底物。酪蛋白对微钙蛋白酶和米钙蛋白酶的K(m)值与其他底物(如 fodrin或MAP2,它们可能是钙蛋白酶的“天然”底物)相似,并且没有理由认为酪蛋白的钙蛋白酶水解与fodrin或MAP2的水解本质上不同,而fodrin或MAP2作为蛋白酶分析的底物则难以获得得多。(4)BODIPY-FL-酪蛋白分析能够检测到10 ng(约5 nM)的钙蛋白酶,并且几乎与迄今为止报道的最灵敏的钙蛋白酶分析一样灵敏。(5)BODIPY-FL-酪蛋白分析与FITC-酪蛋白分析具有相同的重现性,FITC-酪蛋白分析的重现性与用于测定钙蛋白酶活性的其他方法的重现性相当或更好。BODIPY-FL-酪蛋白分析是一种通用的蛋白水解活性分析方法,可用于任何能切割酪蛋白的蛋白酶。