Gołos B, Rode W
Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warszawa.
Acta Biochim Pol. 1999;46(3):837-40.
A new rapid, sensitive and convenient procedure is presented allowing determination of dUTPase activity. With [5-(3)H]dUTP used as the substrate, dUTPase, converts it to the corresponding monophosphate and is coupled with thymidylate synthase-catalyzed reaction, resulting in tritium release from [5-(3)H]dUMP. Following charcoal absorption of the labeled nuleotides, radioactivity of tritiated water is determined. The new assay was tested to show comparable results with a previously described assay, based on measuring dUTPase-catalyzed [5-(3)H]dUMP production.
本文介绍了一种新的快速、灵敏且简便的方法,可用于测定dUTPase活性。以[5-(3)H]dUTP为底物,dUTPase将其转化为相应的单磷酸,并与胸苷酸合成酶催化的反应偶联,导致[5-(3)H]dUMP中的氚释放。在用活性炭吸附标记的核苷酸后,测定氚化水的放射性。基于测量dUTPase催化产生的[5-(3)H]dUMP,对新方法进行了测试,结果显示与先前描述的方法相当。