Cencic Regina, Robert Francis, Pelletier Jerry
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Methods Enzymol. 2007;431:269-302. doi: 10.1016/S0076-6879(07)31013-6.
In eukaryotes, translation initiation is rate-limiting with much regulation exerted at the ribosome recruitment and ternary complex (eIF2.GTP.Met-tRNA(i)(Met)) formation steps. Although small molecule inhibitors have been extremely useful for chemically dissecting translation, there is a dearth of compounds available to study the initiation phase in vitro and in vivo. In this chapter, we describe reverse and forward chemical genetic screens developed to identify new inhibitors of translation. The ability to manipulate cell extracts biochemically, and to compare the activity of small molecules on translation of mRNA templates that differ in their factor requirements for ribosome recruitment, facilitates identification of the relevant target.
在真核生物中,翻译起始是限速步骤,在核糖体招募和三元复合物(eIF2·GTP·Met-tRNA(i)(Met))形成步骤受到多种调控。尽管小分子抑制剂对于从化学角度剖析翻译过程极为有用,但用于在体外和体内研究起始阶段的化合物却很匮乏。在本章中,我们描述了为鉴定新的翻译抑制剂而开发的反向和正向化学遗传学筛选方法。能够对细胞提取物进行生化操作,并比较小分子对核糖体招募所需因子不同的mRNA模板翻译的活性,有助于鉴定相关靶点。