Methods to identify and characterize inhibitors of bacterial RNA polymerase.

A Simon Lynch, Qun Du
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引用次数: 3

Abstract

RNA polymerase is essential to the viability of bacteria in all phases of growth and development and is a proven chemotherapeutic target as the cellular target of the rifamycin class of antibiotics. However, despite the characterization of multiple different classes of natural products that selectively target bacterial RNA polymerase, and the identification of a limited number of synthetic compound inhibitors, only agents of the rifamycin class have been developed and approved for human clinical use as antibiotics. Herein we describe a scintillation proximity assay (SPA) for identifying and characterizing inhibitors of bacterial RNA polymerases and that is applicable to de novo drug discovery programs through application of automated high-throughput screening methods. In addition, we describe gel electrophoresis-based methods that are applicable to the detailed characterization of inhibitors of transcriptional initiation or elongation by bacterial RNA polymerases.

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方法鉴定和表征细菌RNA聚合酶抑制剂。
RNA聚合酶对细菌在生长发育的各个阶段的生存能力至关重要,并且作为利福霉素类抗生素的细胞靶点是一种被证实的化疗靶点。然而,尽管有多种不同类别的天然产物选择性靶向细菌RNA聚合酶,并且鉴定了有限数量的合成化合物抑制剂,但只有利福霉素类药物已被开发并批准作为人类临床使用的抗生素。在此,我们描述了一种用于鉴定和表征细菌RNA聚合酶抑制剂的闪烁接近试验(SPA),该试验通过应用自动化高通量筛选方法适用于新药物发现项目。此外,我们描述了基于凝胶电泳的方法,适用于细菌RNA聚合酶转录起始或延伸抑制剂的详细表征。
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