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Structure of the mammalian 80S ribosome at 8.7 angstrom resolution

机译:8.7埃分辨率的哺乳动物80S核糖体的结构

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摘要

In this paper, we present a structure of the mammalian ribosome determined at similar to 8.7 angstrom resolution by electron cryomicroscopy and single-particle methods. A model of the ribosome was created by docking homology models of subunit rRNAs and conserved proteins into the density map. We then modeled expansion segments in the subunit rRNAs and found unclaimed density for similar to 20 proteins. In general, many conserved proteins and novel proteins interact with expansion segments to form an integrated framework that may stabilize the mature ribosome. Our structure provides a snapshot of the mammalian ribosome at the beginning of translation and lends support to current models in which large movements of the small subunit and L1 stalk occur during tRNA translocation. Finally, details are presented for intersubunit bridges that are specific to the eukaryotic ribosome. We suggest that these bridges may help reset the conformation of the ribosome to prepare for the next cycle of chain elongation.
机译:在本文中,我们介绍了通过电子冷冻显微镜和单颗粒方法测定的类似于8.7埃分辨率的哺乳动物核糖体的结构。通过将亚基rRNA和保守蛋白的同源性模型对接到密度图中来创建核糖体模型。然后,我们对亚基rRNA中的扩增片段进行了建模,发现了类似于20种蛋白质的未知密度。通常,许多保守的蛋白质和新型蛋白质与扩增片段相互作用以形成可以稳定成熟核糖体的整合框架。我们的结构在翻译开始时提供了哺乳动物核糖体的快照,并为当前的模型提供了支持,在tRNA易位期间,小亚基和L1茎发生大量运动。最后,详细介绍了真核生物核糖体特异的亚基间桥。我们建议这些桥可能有助于重置核糖体的构象,为下一轮链延长做准备。

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