Ménard L, Poirier G G
Département de Biologie, Faculté des Sciences, Université de Sherbrooke, Qué., Canada.
Biochem Cell Biol. 1987 Jul;65(7):668-73. doi: 10.1139/o87-088.
We have developed a rapid, highly reproducible assay to determine poly(ADP-ribose) glycohydrolase activity which measures directly the appearance of the reaction product. We also analysed the majority of different techniques which are used to determine poly(ADP-ribose) glycohydrolase activity and found that the apparent activity can vary extensively depending on the method used. Thin-layer chromatography using PEI-F-cellulose was the only method which evaluated directly the specific release of ADP-ribose; by comparison with this method, the other procedures gave an over- or under-estimation of 2- to 10-fold of the enzymatic activity. A rapid method of affinity chromatography has also been developed to synthesize and purify in high yield poly(ADP-ribose) (35% conversion of 1 mM NAD to poly(ADP-ribose)).
我们开发了一种快速、高度可重复的测定方法来测定聚(ADP-核糖)糖苷水解酶活性,该方法直接测量反应产物的出现。我们还分析了用于测定聚(ADP-核糖)糖苷水解酶活性的大多数不同技术,发现表观活性会因所使用的方法而有很大差异。使用PEI-F-纤维素的薄层色谱法是唯一直接评估ADP-核糖特异性释放的方法;与该方法相比,其他程序对酶活性的估计高估或低估了2至10倍。还开发了一种快速亲和色谱方法,以高产率合成和纯化聚(ADP-核糖)(1 mM NAD转化为聚(ADP-核糖)的转化率为35%)。