Cook L, Schafer-Mitchell M, Angle C, Stohs S
J Chromatogr. 1985 May 3;339(2):293-301. doi: 10.1016/s0378-4347(00)84656-3.
We report a rapid and reproducible assay for activity of human erythrocyte pyrimidine 5'-nucleotidase and deoxypyrimidine 5'-nucleotidase. The nucleotides CMP, UMP, dUMP, dCMP or dTMP are individually incubated 30 min at 37 degrees C with erythrocyte hemolysate and 4 mM magnesium chloride in Tris, pH 7.5. Data are provided for standardization of the reaction with each substrate. Individual nucleoside products are assayed in less than 10 min by reversed-phase high-performance liquid chromatography at 280 nm with 0-14% methanol in 0.01 M potassium dihydrogen phosphate. This is the first report of a high-performance liquid chromatographic assay system which allows quantitation of the activity of pyrimidine 5'-nucleotidase isozymes using five individual pyrimidine and deoxypyrimidine nucleotides as the substrates.
我们报告了一种用于检测人红细胞嘧啶5'-核苷酸酶和脱氧嘧啶5'-核苷酸酶活性的快速且可重复的方法。将核苷酸CMP、UMP、dUMP、dCMP或dTMP分别与红细胞溶血产物以及Tris(pH 7.5)中4 mM氯化镁在37℃孵育30分钟。提供了与每种底物反应标准化的数据。通过在280 nm处使用0.01 M磷酸二氢钾中含0 - 14%甲醇的反相高效液相色谱法,在不到10分钟内对各个核苷产物进行检测。这是首次报道一种高效液相色谱检测系统,该系统能够使用五种单个嘧啶和脱氧嘧啶核苷酸作为底物来定量嘧啶5'-核苷酸酶同工酶的活性。