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Alternative Mode of E-Site tRNA Binding in the Presence of a Downstream mRNA Stem Loop at the Entrance Channel

机译:在入口通道的下游mRNA阀门圈存在下,E-位点TRNA结合的替代模式

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摘要

Structured mRNAs positioned downstream of the ribosomal decoding center alter gene expression by slowing protein synthesis. Here, we solved the cryo-EM structure of the bacterial ribosome bound to an mRNA containing a 30 stem loop that regulates translation. Unexpectedly, the E-site tRNA adopts two distinct orientations. In the first structure, normal interactions with the 50S and 30S E site are observed. However, in the second structure, although the E-site tRNA makes normal interactions with the 50S E site, its anticodon stem loop moves similar to 54 angstrom away from the 30S E site to interact with the 30S head domain and 50S uL5. This position of the E-site tRNA causes the uL1 stalk to adopt a more open conformation that likely represents an intermediate state during E-site tRNA dissociation. These results suggest that structured mRNAs at the entrance channel restrict 30S subunit movement required during translation to slow E-site tRNA dissociation.
机译:通过减缓蛋白质合成的结构化MRNA位于核糖体解码中心的下游改变基因表达。 在这里,我们解决了与含有30个茎环的mRNA结合的细菌核糖体的冷冻核心结构,该茎环调节翻译。 出乎意料地,电子网站TRNA采用两个不同的取向。 在第一结构中,观察到与50S和30S E位点的正常相互作用。 然而,在第二结构中,虽然E-站点TRNA与50s E位点进行正常相互作用,但其抗oconon杆环移动到54埃远离30S E位点以与30S头部域和50s UL5相互作用。 E-TABTNA的该位置使UL1茎通过更开放的构象采用,这可能代表E-位点的TRNA解离过程中的中间状态。 这些结果表明,入口通道的结构化MRNA限制在翻译期间需要30S所需的30S亚基运动,以慢速度TRNA解离。

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