Noton Sarah L, Ludeke Barbara
Department of Virology, Immunology & Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Methods Mol Biol. 2025;2948:181-194. doi: 10.1007/978-1-0716-4666-3_12.
Here, we detail a biochemical assay that assesses respiratory syncytial virus (RSV) RNA-dependent RNA polymerase activities at the viral promoters in vitro. The assay consists of a purified recombinant RSV polymerase complex comprising the L protein and its cofactor P, combined with a short RNA template and radiolabeled NTPs. RNA synthesis by the L-P complex yields radiolabeled RNA products that can be separated at the nucleotide level on denaturing polyacrylamide gels and detected by autoradiography or phosphor image analysis. Each component of the assay can be readily manipulated. As such, this simple assay has aided the understanding of early polymerase transcription and genome synthesis initiation events, revealed previously unknown polymerase functions, and determined how various RSV polymerase inhibitors function.
在此,我们详细介绍一种生化检测方法,该方法可在体外评估呼吸道合胞病毒(RSV)在病毒启动子处的RNA依赖性RNA聚合酶活性。该检测方法由一个纯化的重组RSV聚合酶复合物组成,该复合物包含L蛋白及其辅因子P,并结合一个短RNA模板和放射性标记的NTP。L-P复合物合成的RNA会产生放射性标记的RNA产物,这些产物可在变性聚丙烯酰胺凝胶上按核苷酸水平进行分离,并通过放射自显影或磷图像分析进行检测。该检测方法的每个组分都易于操作。因此,这种简单的检测方法有助于理解早期聚合酶转录和基因组合成起始事件,揭示了以前未知的聚合酶功能,并确定了各种RSV聚合酶抑制剂的作用机制。