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The Native 3D Organization of Bacterial Polysomes

机译:细菌多核糖体的原生3D组织

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Recent advances have led to insights into the structure of the bacterial ribosome, but little is known about the 3D organization of ribosomes in the context of translating polysomes. We employed cryoelectron tomography and a template-matching approach to map 70S ribosomes in vitrified bacterial translation extracts and in lysates of active E. coil spheroplasts. In these preparations, polysomal arrangements were observed in which neighboring ribosomes are densely packed and exhibit preferred orientations. Analysis of characteristic examples of polysomes reveals a staggered or pseudohelical organization of ribosomes along the mRNA trace, with the transcript being sequestered on the inside, the tRNA entrance sites being accessible, and the polypeptide exit sites facing the cytosol. Modeling of elongating nascent polypeptide chains suggests that this arrangement maximizes the distance between nascent chains on adjacent ribosomes, thereby reducing the probability of intermolecular interactions that would give rise to aggregation and limit productive folding.
机译:最近的进展已经导致对细菌核糖体结构的见解,但是在翻译多核糖体的背景下对核糖体的3D组织了解甚少。我们采用了冷冻电子断层扫描和模板匹配的方法,在玻璃化细菌翻译提取物和活性大肠杆菌原生质球的裂解物中绘制了70S核糖体图。在这些制剂中,观察到多核体排列,其中相邻的核糖体被密集堆积并表现出优选的取向。对多核糖体特征性实例的分析显示,核糖体沿mRNA轨迹呈交错或假螺旋状组织,转录物被隔离在内部,tRNA入口位点可及,而多肽出口位点面向细胞质。伸长的新生多肽链的建模表明,这种排列使相邻核糖体上新生链之间的距离最大,从而降低了分子间相互作用的可能性,这种相互作用会引起聚集并限制生产性折叠。

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