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利用聚合酶的混杂性:一种简单的比色法RNA聚合酶测定法。

Exploiting polymerase promiscuity: A simple colorimetric RNA polymerase assay.

作者信息

Vassiliou W, Epp J B, Wang B B, Del Vecchio A M, Widlanski T, Kao C C

机构信息

Department of Biology, Indiana University, Bloomington, Indiana 47405, USA.

出版信息

Virology. 2000 Sep 1;274(2):429-37. doi: 10.1006/viro.2000.0492.

Abstract

We developed a convenient colorimetric assay for monitoring RNA synthesis from DNA-dependent RNA polymerases (DdRp) and viral RNA-dependent RNA polymerases (RdRp). ATP and GTP with a p-nitrophenyl moiety attached to the gamma-phosphate were synthesized (PNP-NTPs). These PNP-NTPs can be used for RNA synthesis by several RNA polymerases, including the RdRps from brome mosaic virus and bovine viral diarrhea virus and the DdRps from bacteriophage T7 and SP6. When the polymerase reactions were performed in the presence of alkaline phosphatase, which digests the p-nitrophenylpyrophosphate side-product of phosphoryl transfer to the chromogenic p-nitrophenylate, an increase in absorbence at 405 nm was observed. These nucleotide analogues were used in continuous colorimetric monitoring of polymerase activity. Furthermore, the PNP-NTPs were found to be stable and utilized by RNA polymerases in the presence of human plasma. This simple colorimetric polymerase assay can be performed in a standard laboratory spectrophotometer and will be useful in screens for inhibitors of viral RNA synthesis.

摘要

我们开发了一种便捷的比色测定法,用于监测依赖DNA的RNA聚合酶(DdRp)和病毒依赖RNA的RNA聚合酶(RdRp)的RNA合成。合成了在γ-磷酸上连接有对硝基苯基部分的ATP和GTP(PNP-NTPs)。这些PNP-NTPs可用于多种RNA聚合酶的RNA合成,包括来自雀麦花叶病毒和牛病毒性腹泻病毒的RdRp以及来自噬菌体T7和SP6的DdRp。当在碱性磷酸酶存在下进行聚合酶反应时,碱性磷酸酶会消化磷酸转移的对硝基苯基焦磷酸副产物生成显色的对硝基苯酚盐,此时在405 nm处吸光度增加。这些核苷酸类似物用于聚合酶活性的连续比色监测。此外,发现PNP-NTPs在人血浆存在下是稳定的且能被RNA聚合酶利用。这种简单的比色聚合酶测定法可在标准实验室分光光度计中进行,将有助于筛选病毒RNA合成抑制剂。

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