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DOI: 10.3791/58100-v
Antonio E. Chambers*1, Adam E. Richardson*1, David F. Read2, Thomas J. Waller3, Douglas A. Bernstein1, Philip J. Smaldino1
1Department of Biology,Ball State University, 2Department of Genome Sciences,University of Washington, 3Department of Molecular, Cellular, and Developmental Biology,University of Michigan
Please note that some of the translations on this page are AI generated. Click here for the English version.
This article presents a protocol for the biochemical characterization of the yeast RNA-modifying enzyme Mod5, focusing on tRNA-isopentenyl transferase activity. The method is designed for in-vitro detection and characterization of this enzyme's activity, providing a straightforward assay for RNA modification.
在这里, 我们描述了一个协议的生化特性的酵母 rna 修饰酶, Mod5, 并讨论如何将该协议适用于其他 RNA 修饰酶。
该协议的总体目标是在振动中对tRNA-Isopentenyl转移酶活性进行生化特征。该方法对纯化重组酶的tRNA-isopentenyl转移酶活性的体外检测和表征非常有用。该技术的主要优点是,它是一种简单而直接的检测,用于检测共价RNA修饰。
虽然这种方法为tRNA-isopentenyl转移酶活性提供了见解,但它对于广范围或RNA修改酶的生化特性具有潜在的适应性。本程序的第一步是彻底清洁用于铸造凝胶的玻璃板。用肥皂和水清洗盘子,用去离子水冲洗好,然后用异丙醇和无绒湿巾清洗盘子。
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