Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8562, Japan.
Laboratory for Cell-Free Protein Synthesis, RIKEN Quantitative Biology Center, Suita, Osaka 565-0874, Japan.
RNA. 2018 Nov;24(11):1512-1519. doi: 10.1261/rna.065615.118. Epub 2018 Aug 3.
Reconstitution of ribosomes in vitro from individual ribosomal proteins provides a powerful tool for understanding the ribosome assembly process including the sequential incorporation of ribosomal proteins. However, conventional assembly methods require high-salt conditions for efficient ribosome assembly. In this study, we reconstituted 30S ribosomal subunits from individually purified ribosomal proteins in the presence of ribosome biogenesis factors. In this system, two GTPases (Era and YjeQ) facilitated assembly of a 30S subunit exhibiting poly(U)-directed polyphenylalanine synthesis and native protein synthesis under physiological conditions. This in vitro system permits a study of the assembly process and function of ribosome biogenesis factors, and it will facilitate the generation of ribosomes from DNA without using cells.
从单个核糖体蛋白体外重建核糖体为理解核糖体组装过程(包括核糖体蛋白的顺序掺入)提供了强有力的工具。然而,传统的组装方法需要高盐条件才能有效地进行核糖体组装。在这项研究中,我们在核糖体生物发生因子的存在下,从单独纯化的核糖体蛋白中重新组装 30S 核糖体亚基。在这个系统中,两种 GTPases(Era 和 YjeQ)促进了一个 30S 亚基的组装,该亚基在生理条件下表现出多聚(U)指导的多苯丙氨酸合成和天然蛋白质合成。该体外系统允许研究核糖体生物发生因子的组装过程和功能,并将有助于在不使用细胞的情况下从 DNA 生成核糖体。