Hori Hiroyuki
Department of Materials Science and Biotechnology, Graduate School of Sciences and Engineering, Ehime University, Ehime, Japan.
Methods Mol Biol. 2010;607:173-85. doi: 10.1007/978-1-60327-331-2_15.
Cell-free translation systems are a powerful tool for the production of many kinds of proteins. However, there are some barriers to improve the system in order to make it a more convenient approach. These include the fact that the production of proteins made up of hetero subunits is difficult. In this chapter, we describe the synthesis of yeast tRNA (m(7)G46) methyltransferase as a model protein. This enzyme catalyzes transfer of a methyl group from S-adenosyl-L-methionine to guanine at position 46 in tRNA and generates N(7)-methylguanine. Yeast tRNA (m(7)G46) methyltransferase is composed of two protein subunits, Trm8 and Trm82. To obtain the active Trm8-Trm82 complex, co-translation of both subunits is necessary. Preparation of mRNAs, in vitro synthesis and purification of the complex are explained in this chapter.
无细胞翻译系统是生产多种蛋白质的强大工具。然而,为了使其成为一种更便捷的方法,在改进该系统方面存在一些障碍。其中包括由异源亚基组成的蛋白质生产困难这一事实。在本章中,我们描述了酵母tRNA(m(7)G46)甲基转移酶作为一种模型蛋白的合成。该酶催化将甲基从S-腺苷-L-甲硫氨酸转移到tRNA中第46位的鸟嘌呤上,并生成N(7)-甲基鸟嘌呤。酵母tRNA(m(7)G46)甲基转移酶由两个蛋白质亚基Trm8和Trm82组成。为了获得有活性的Trm8-Trm82复合物,两个亚基的共翻译是必要的。本章解释了mRNA的制备、复合物的体外合成和纯化。