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Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways

机译:GE81112阻止的30S预启动复合物的结构揭示了细菌和真核蛋白合成起始途径中的结构相似之处

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摘要

In bacteria, the start site and the reading frame of the messenger RNA are selected by the small ribosomal subunit (30S) when the start codon, typically an AUG, is decoded in the P-site by the initiator tRNA in a process guided and controlled by three initiation factors. This process can be efficiently inhibited by GE81112, a natural tetrapeptide antibiotic that is highly specific toward bacteria. Here GE81112 was used to stabilize the 30S pre-initiation complex and obtain its structure by cryo-electron microscopy. The results obtained reveal the occurrence of changes in both the ribosome conformation and initiator tRNA position that may play a critical role in controlling translational fidelity. Furthermore, the structure highlights similarities with the early steps of initiation in eukaryotes suggesting that shared structural features guide initiation in all kingdoms of life.
机译:在细菌中,当起始密码子(通常为AUG)由起始tRNA在引导和控制的过程中在p位点解码时,信使RNA的起始位点和阅读框由小核糖体亚基(30S)选择。通过三个启动因素。 GE81112是一种对细菌具有高度特异性的天然四肽抗生素,可有效抑制该过程。在这里,GE81112用于稳定30S预引发复合物,并通过冷冻电子显微镜获得其结构。获得的结果揭示了核糖体构象和起始子tRNA位置变化的发生,这可能在控制翻译保真度中起关键作用。此外,该结构突显了与真核生物起始阶段的相似之处,这表明共享的结构特征指导了所有生命王国的起始。

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