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首页> 外文期刊>Journal of Molecular Biology >A comparison of the yeast and rabbit 80 S ribosome reveals the topology of the nascent chain exit tunnel, inter-subunit bridges and mammalian rRNA expansion segments.
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A comparison of the yeast and rabbit 80 S ribosome reveals the topology of the nascent chain exit tunnel, inter-subunit bridges and mammalian rRNA expansion segments.

机译:酵母和兔80 S核糖体的比较揭示了新生链出口隧道,亚基间桥和哺乳动物rRNA扩展片段的拓扑。

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Protein synthesis in eukaryotes is mediated by both cytoplasmic and membrane-bound ribosomes. During the co-translational translocation of secretory and membrane proteins, eukaryotic ribosomes dock with the protein conducting channel of the endoplasmic reticulum. An understanding of these processes will require the detailed structure of a eukaryotic ribosome. To this end, we have compared the three-dimensional structures of yeast and rabbit ribosomes at 24 A resolution. In general, we find that the active sites for protein synthesis and translocation have been highly conserved. It is interesting that a channel was visualized in the neck of the small subunit whose entrance is formed by a deep groove. By analogy with the prokaryotic small subunit, this channel may provide a conserved portal through which mRNA is threaded into the decoding center. In addition, both the small and large subunits are built around a dense tubular network. Our analysis further suggests that the nascent chain exit tunnel and the docking surface for the endoplasmic reticulum channel are formed by this network. We surmise that many of these features correspond to rRNA, based on biochemical and structural data.Ribosomal function is critically dependent on the specific association of small and large subunits. Our analysis of eukaryotic ribosomes reveals four conserved inter-subunit bridges with a geometry similar to that found in prokaryotes. In particular, a double-bridge connects the small subunit platform with the interface canyon on the large subunit. Moreover, a novel bridge is formed between the platform and the base of the L1 domain. Finally, size differences between mammalian and yeast large subunit rRNAs have been correlated with five expansion segments that form two large spines and three extended fingers. Overall, we find that expansion segments within the large subunit rRNA have been incorporated at positions distinct from the active sites for protein synthesis and translocation. Copyright 2000 Academic Press.
机译:真核生物中的蛋白质合成是由细胞质和膜结合的核糖体介导的。在分泌和膜蛋白的共翻译易位过程中,真核核糖体与内质网的蛋白传导通道对接。对这些过程的理解将需要真核生物核糖体的详细结构。为此,我们比较了24 A分辨率的酵母和兔核糖体的三维结构。通常,我们发现蛋白质合成和易位的活性位点高度保守。有趣的是,在小亚基的脖子上看到了一个通道,该通道的入口由一个深槽形成。类似于原核小亚基,该通道可以提供保守的门户,通过该门户,mRNA可以穿入解码中心。此外,小型和大型子单元都围绕密集的管状网络构建。我们的分析进一步表明,该网络形成了新生的链出口隧道和内质网通道的对接表面。根据生化和结构数据,我们推测其中许多特征与rRNA相对应。核糖体功能严重依赖于大小亚基的特定关联。我们对真核生物核糖体的分析揭示了四个保守的亚基间桥,其几何形状与原核生物相似。特别是,双桥将小型子单元平台与大型子单元上的接口峡谷相连。此外,在平台和L1域的基础之间形成了一个新颖的桥梁。最后,哺乳动物和酵母大亚基rRNA之间的大小差异已与形成两个大棘和三个延伸手指的五个扩展片段相关。总的来说,我们发现大亚基rRNA内的扩增片段已被整合到不同于蛋白质合成和易位活性位点的位置。版权所有2000学术出版社。

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