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Structural insights into eukaryotic ribosomes and the initiation of translation

机译:真核生物核糖体的结构见解和翻译的启动

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摘要

The initiation of protein biosynthesis entails the ordered assembly of elongation-competent ribosomes, with an initiator tRNA basepaired to an appropriate mRNA start codon. In eukaryotes, this process is more complex than in prokaryotes and involves numerous protein factors that mediate tRNA delivery, mRNA binding, start codon selection and subunit joining. The recent 40S:eIF1, 80S and eIF2:tRNA:GDPNP ternary complex structures provide an initial structural framework toward a molecular understanding of the eukaryotic translation initiation process. Updated homology models of larger initiation complexes provide first insights into the likely arrangements of these higher-order complexes, but also reveal the limits of our current understanding of the eukaryotic translation initiation process.
机译:蛋白质生物合成的启动需要具有延伸能力的核糖体的有序组装,其中启动子tRNA碱基配对至合适的mRNA起始密码子。在真核生物中,此过程比原核生物中的复杂得多,并且涉及许多介导tRNA传递,mRNA结合,起始密码子选择和亚基连接的蛋白质因子。最近的40S:eIF1、80S和eIF2:tRNA:GDPNP三元复合结构为分子对真核翻译起始过程的理解提供了一个初始的结构框架。较大的起始复合物的更新的同源性模型提供了对这些高阶复合物的可能排列的初步见解,但也揭示了我们目前对真核翻译起始过程的理解的局限性。

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