Suppr超能文献

检测干扰脱氧核糖核苷5'-三磷酸酶促测定的活性。

Detection of activities that interfere with the enzymatic assay of deoxyribonucleoside 5'-triphosphates.

作者信息

North T W, Bestwick R K, Mathews C K

出版信息

J Biol Chem. 1980 Jul 25;255(14):6640-5.

PMID:6248528
Abstract

Several enzymes that interfere with the enzymatic assay of deoxyribonucleoside 5'-triphosphates (dNTP's) are present as contaminants when nucleotides are extracted from HeLa cells with 60% methanol. These activities include a nuclease, nucleoside diphosphokinase, and deoxyribonucleoside monophosphokinases which phosphorylate dAMP, dGMP, and dCMP. Collectively, these enzymes are able to degrade and reutilize the DNA template which is used together with DNA polymerase for dNTP assays. This process introduces large errors when dNTP assays are performed in this manner. Attempts to block the enzymatic conversion of deoxyribonucleoside diphosphates to triphosphates by inhibition of nucleoside diphosphokinase were unsuccessful because of the inability to block completely the kinase activity. Acid extraction of nucleotides also results in the presence of an activity that interferes with the enzymatic dNTP assay. The error introduced by this interfering activity is much smaller than that arising from the enzymes present in methanol extracts. All of these interfering activities are removed when cells are first extracted with 60% methanol and the resulting extract is subsequently treated with perchloric acid.

摘要

当用60%甲醇从HeLa细胞中提取核苷酸时,有几种会干扰脱氧核糖核苷5'-三磷酸(dNTP)酶促测定的酶作为污染物存在。这些活性包括一种核酸酶、核苷二磷酸激酶以及能使dAMP、dGMP和dCMP磷酸化的脱氧核糖核苷单磷酸激酶。这些酶共同作用,能够降解并重新利用与DNA聚合酶一起用于dNTP测定的DNA模板。当以这种方式进行dNTP测定时,这个过程会引入很大的误差。由于无法完全阻断激酶活性,试图通过抑制核苷二磷酸激酶来阻断脱氧核糖核苷二磷酸向三磷酸的酶促转化未成功。核苷酸的酸提取也会导致存在一种干扰dNTP酶促测定的活性。这种干扰活性引入的误差比甲醇提取物中存在的酶所产生的误差小得多。当细胞先用60%甲醇提取,然后将所得提取物用高氯酸处理时,所有这些干扰活性都会被去除。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验