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一种用于核糖核酸酶H活性的毛细管电泳测定法。

A capillary electrophoretic assay for ribonuclease H activity.

作者信息

Chan King C, Budihas Scott R, Le Grice Stuart F J, Parniak Michael A, Crouch Robert J, Gaidamakov Sergei A, Isaaq Haleem J, Wamiru Antony, McMahon James B, Beutler John A

机构信息

Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc., Center for Cancer Research, NCI at Frederick, Frederick, MD 21702, USA.

出版信息

Anal Biochem. 2004 Aug 15;331(2):296-302. doi: 10.1016/j.ab.2004.05.017.

Abstract

A capillary electrophoretic assay was developed to measure the ribonuclease (RNase) H activity of human immunodeficiency virus (HIV) type 1 reverse transcriptase. Cleavage of a fluorescein-labeled RNA-DNA heteroduplex was monitored by capillary electrophoresis. This new assay was used as a secondary assay to confirm hits from a high-throughput screening program. Since autofluorescent compounds in samples migrated differently from both substrate and product in most cases, the assay was extremely robust for assaying enzymatic inhibition of such samples, in contrast to a simple well-based approach. The assay was broadly applicable to other RNases H, specifically those from human, Escherichia coli, and HIV-2, although product profiles varied for each enzyme.

摘要

开发了一种毛细管电泳测定法来测量1型人类免疫缺陷病毒(HIV)逆转录酶的核糖核酸酶(RNase)H活性。通过毛细管电泳监测荧光素标记的RNA-DNA异源双链体的切割。这种新测定法用作二级测定法,以确认高通量筛选程序中的命中结果。由于在大多数情况下,样品中的自发荧光化合物与底物和产物的迁移方式不同,与简单的基于孔板的方法相比,该测定法在测定此类样品的酶抑制方面极其稳健。该测定法广泛适用于其他RNase H,特别是来自人类、大肠杆菌和HIV-2的RNase H,尽管每种酶的产物图谱有所不同。

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