Jong A Y, Yu K, Zhou B, Frgala T, Reynolds C P, Yen Y
Department of Pediatrics, Childrens Hospital of Los Angeles and the University of Southern California School of Medicine, 90027, USA. ajong%
J Biomed Sci. 1998;5(1):62-8. doi: 10.1007/BF02253357.
Ribonucleotide reductase (RR) is a key regulatory enzyme in the DNA synthesis pathway and is the target of the cancer chemotherapeutic agent hydroxyurea. The study of RR is significantly hindered by the tedious and labor-intensive nature of enzymatic assay. In this report, we present a novel RR assay in which detection of the deoxyribonucleotides produced by RR occurs via coupling to the DNA polymerase reaction, and is enhanced by using RNase to degrade endogenous RNA. Cell extracts from various cell lines were treated with RNase and then reacted with ATP and radioactive ribonucleotide diphosphate as the substrate. Incorporation of the radioactive substrate [14C]CDP into DNA was linear over 30 min and was linear with the amount of extract, which provided RR activity. The reaction was inhibited by hydroxyurea and required Mg2+ and ATP, suggesting that the assay is specific to RR activity. While RR activities determined by our method and by a conventional method were comparable, this novel method proved to be simpler, faster, more sensitive and less expensive. In addition, assay of the RR activity for multiple samples can easily be performed simultaneously. It is superior to other RR assays in all aspects.
核糖核苷酸还原酶(RR)是DNA合成途径中的关键调节酶,也是癌症化疗药物羟基脲的作用靶点。RR的研究因酶活性测定的繁琐和劳动密集性质而受到显著阻碍。在本报告中,我们提出了一种新型的RR测定方法,其中通过与DNA聚合酶反应偶联来检测RR产生的脱氧核苷酸,并通过使用核糖核酸酶降解内源性RNA来增强检测。来自各种细胞系的细胞提取物用核糖核酸酶处理,然后与ATP和放射性核糖核苷酸二磷酸作为底物反应。放射性底物[14C]CDP掺入DNA在30分钟内呈线性,并且与提供RR活性的提取物量呈线性关系。该反应被羟基脲抑制,并且需要Mg2+和ATP,这表明该测定对RR活性具有特异性。虽然通过我们的方法和传统方法测定的RR活性相当,但这种新方法被证明更简单、更快、更灵敏且成本更低。此外,可以轻松同时对多个样品进行RR活性测定。它在各个方面都优于其他RR测定方法。