Minina Elena A, Stael Simon, Van Breusegem Frank, Bozhkov Peter V
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Uppsala, Sweden.
Methods Mol Biol. 2014;1133:237-53. doi: 10.1007/978-1-4939-0357-3_15.
Metacaspases are essential for cell death regulation in plants. Further understanding of biochemistry of metacaspases and their molecular function in plant biology requires a set of robust methods for detection of metacaspase activation and quantitative analysis of corresponding proteolytic activity. Here we describe methods for purification of recombinant metacaspases, measurement of enzymatic activity of recombinant and endogenous metacaspases in vitro and in cell lysates, respectively, and finally detection of metacaspase activation in vivo. Additionally, an in vitro metacaspase protein substrate cleavage assay based on the cell-free production of substrate protein followed by proteolysis with recombinant metacaspase is presented. These methods have been originally developed for type II metacaspases from Arabidopsis and Norway spruce (Picea abies), but they can be used as templates for type I metacaspases, as well as for type II metacaspases from other species.
类半胱天冬酶对于植物细胞死亡调控至关重要。要进一步了解类半胱天冬酶的生物化学及其在植物生物学中的分子功能,需要一套可靠的方法来检测类半胱天冬酶的激活情况并对相应的蛋白水解活性进行定量分析。在此,我们描述了重组类半胱天冬酶的纯化方法、分别在体外和细胞裂解物中测量重组和内源性类半胱天冬酶的酶活性的方法,以及最后在体内检测类半胱天冬酶激活的方法。此外,还介绍了一种基于无细胞生产底物蛋白然后用重组类半胱天冬酶进行蛋白水解的体外类半胱天冬酶蛋白底物切割试验。这些方法最初是针对拟南芥和挪威云杉(云杉)的II型类半胱天冬酶开发的,但它们可作为I型类半胱天冬酶以及其他物种II型类半胱天冬酶的模板。