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一种基于考马斯亮蓝G-250的比色测定法,用于测量钙蛋白酶和其他蛋白酶的活性。

A Coomassie brilliant blue G-250-based colorimetric assay for measuring activity of calpain and other proteases.

作者信息

Buroker-Kilgore M, Wang K K

机构信息

Department of Pharmacology, Parke-Davis Pharmaceutical Research, Warner-Lambert Company, Ann Arbor, Michigan 48105.

出版信息

Anal Biochem. 1993 Feb 1;208(2):387-92. doi: 10.1006/abio.1993.1066.

Abstract

The activity of cytosolic calcium-dependent neutral protease (calpain) is commonly measured using casein as a substrate. A novel, modified caseinolysis assay is now developed. It involves incubation of calpain with substrate casein, followed by removal of an aliquot to which Coomassie brilliant blue G-250 dye reagent is added. The assay is based on the observation that the dye interacts only with protein but not the proteolytic products (small peptides and amino acids). Unlike the existing caseinolysis assay, this novel assay does not require separation of substrate from products and measurement is done in the visible range (595 nm). It is also more sensitive than existing colorimetric assays which use dye-conjugated protein substrates. The assay can also be used to measure the activity of other proteases such as trypsin and papain.

摘要

胞质钙依赖性中性蛋白酶(钙蛋白酶)的活性通常以酪蛋白作为底物进行测定。目前已开发出一种新型的改良酪蛋白水解测定法。该方法包括将钙蛋白酶与底物酪蛋白一起孵育,然后取出一份样品,向其中加入考马斯亮蓝G - 250染料试剂。该测定法基于这样的观察结果:染料仅与蛋白质相互作用,而不与蛋白水解产物(小肽和氨基酸)相互作用。与现有的酪蛋白水解测定法不同,这种新型测定法不需要将底物与产物分离,并且在可见光范围(595 nm)内进行测量。它也比使用染料偶联蛋白底物的现有比色测定法更灵敏。该测定法还可用于测量其他蛋白酶的活性,如胰蛋白酶和木瓜蛋白酶。

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