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一种用于分离抑制原核RNA聚合酶组装的化合物的多孔分析方法。

A multiwell assay to isolate compounds inhibiting the assembly of the prokaryotic RNA polymerase.

作者信息

André Estelle, Bastide Lionel, Villain-Guillot Philippe, Latouche Jaqueline, Rouby Joelle, Leonetti Jean-Paul

机构信息

CNRS UMR 5160 Faculté de Pharmacie, Montpellier, France.

出版信息

Assay Drug Dev Technol. 2004 Dec;2(6):629-35. doi: 10.1089/adt.2004.2.629.

Abstract

We have developed a multiwell assay for the detection of modulators of prokaryotic transcription based on the quantification of protein-protein interaction. This assay consists of three steps: (a) the immobilization of the Escherichia coli protein sigma70 in the well, (b) the incubation of the immobilized protein with core RNA polymerase and a potential inhibitor, and (c) washing and quantification of the binding of core to sigma70 with a monoclonal antibody conjugated to horseradish peroxidase. We show that this assay is sensitive, reproducible, and robust, and is able to discriminate between control competitors with different affinities. We demonstrate the usefulness of the assay to screen for microbial RNA polymerase inhibitors as potential new drugs for the treatment of emerging antibiotic-resistant bacteria.

摘要

我们基于蛋白质-蛋白质相互作用的定量分析,开发了一种用于检测原核转录调节剂的多孔分析方法。该分析方法包括三个步骤:(a) 将大肠杆菌蛋白质sigma70固定在孔中;(b) 将固定化的蛋白质与核心RNA聚合酶及一种潜在抑制剂一起孵育;(c) 用与辣根过氧化物酶偶联的单克隆抗体洗涤并定量核心与sigma70的结合。我们表明该分析方法灵敏、可重复且稳健,能够区分具有不同亲和力的对照竞争物。我们证明了该分析方法在筛选微生物RNA聚合酶抑制剂作为治疗新出现的抗生素耐药细菌的潜在新药方面的实用性。

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