Koshy P J, Rowan A D, Life P F, Cawston T E
School of Clinical and Medical Sciences, University of Newcastle upon Tyne, Newcastle upon Tyne, NE2 4HH, United Kingdom.
Anal Biochem. 1999 Nov 15;275(2):202-7. doi: 10.1006/abio.1999.4310.
We describe two alternative assays for measuring collagenolytic activity using (3)H-acetylated collagen. Both assays have been developed for the 96-well plate format and measure the amount of radiolabeled collagen fragments released into the supernatant from an insoluble (3)H-acetylated collagen fibril preparation. The first method separates digested solubilized fragments from the intact fibril by sedimentation of the undigested collagen by centrifugation. The second method achieves this separation by filtration of the supernatant through the membrane of a 96-well filtration plate which retains the undigested collagen fibril. Both methods give linear dose- and time-dependent responses of collagenase activity > or = 70% of total collagen lysis. In addition, both assays can be simply modified to measure tissue inhibitors of metalloproteinases (TIMPs) inhibitory activity, which is also linear between 20 and 75% of total collagen lysis with the amount of TIMP added.
我们描述了两种使用³H - 乙酰化胶原蛋白测量胶原酶活性的替代检测方法。这两种检测方法均针对96孔板形式开发,用于测量从不溶性³H - 乙酰化胶原纤维制剂释放到上清液中的放射性标记胶原片段的量。第一种方法是通过离心使未消化的胶原蛋白沉淀,将消化后的溶解片段与完整的纤维分离。第二种方法是通过将上清液通过96孔过滤板的膜进行过滤来实现这种分离,该膜可保留未消化的胶原纤维。两种方法对胶原酶活性均呈现线性剂量和时间依赖性反应,占总胶原溶解的≥70%。此外,两种检测方法均可简单修改以测量金属蛋白酶组织抑制剂(TIMPs)的抑制活性,其在添加的TIMP量与总胶原溶解的20%至75%之间也呈线性关系。