Lee Muhoon, Takeuchi-Tomita Nono
Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, Japan.
Methods Mol Biol. 2023;2661:233-255. doi: 10.1007/978-1-0716-3171-3_14.
Mammalian mitochondria have their own dedicated protein synthesis system, which produces 13 essential subunits of the oxidative phosphorylation complexes. Here, we describe the in vitro reconstitution of the mammalian mitochondrial translation system, utilizing purified recombinant mitochondrial translation factors, 55S ribosomes from pig liver mitochondria, and a heterologous yeast tRNA mixture. The system is capable of translating leaderless mRNAs encoding model proteins, such as nanoluciferase with a molecular weight of 19 kDa, and is readily applicable for in vitro evaluations of mRNAs and nascent peptide chain sequences, as well as factors and small molecules that affect mitochondrial translation.
哺乳动物线粒体拥有自己专门的蛋白质合成系统,该系统可产生氧化磷酸化复合物的13个必需亚基。在此,我们描述了哺乳动物线粒体翻译系统的体外重建,利用纯化的重组线粒体翻译因子、猪肝线粒体的55S核糖体和异源酵母tRNA混合物。该系统能够翻译编码模型蛋白的无引导mRNA,如分子量为19 kDa的纳米荧光素酶,并且很容易应用于mRNA和新生肽链序列的体外评估,以及影响线粒体翻译的因子和小分子的体外评估。