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基于大肠杆菌核糖体冷冻电子显微镜的蛋白质合成模型。

A model of protein synthesis based on cryo-electron microscopy of the E. coli ribosome.

作者信息

Frank J, Zhu J, Penczek P, Li Y, Srivastava S, Verschoor A, Radermacher M, Grassucci R, Lata R K, Agrawal R K

机构信息

Wadsworth Center, New York State Department of Health, Albany 12201-0509, USA.

出版信息

Nature. 1995 Aug 3;376(6539):441-4. doi: 10.1038/376441a0.

Abstract

The ribosome is formed by assembly of proteins and nucleic acids, and synthesizes proteins according to genetic instructions in all organisms. Many of the biochemical steps of this fundamental process are known, but a detailed understanding requires a well-defined structural model of the ribosome. Electron microscopy combined with image reconstruction of two-dimensional crystals or single ribosomes has been the most promising technique, but the resolution of the resulting models has been insufficient. Here we report a 25-A reconstruction of the ribosome from Escherichia coli, obtained by combining 4,300 projections of ice-embedded single particles. Our new reconstruction reveals a channel in the small ribosomal subunit and a bifurcating tunnel in the large subunit which may constitute pathways for the incoming message and the nascent polypeptide chain, respectively. Based on these new findings, a three-dimensional model of the basic framework of protein synthesis is presented.

摘要

核糖体由蛋白质和核酸组装而成,在所有生物体中根据遗传指令合成蛋白质。这个基本过程的许多生化步骤已为人所知,但要详细了解则需要核糖体的明确结构模型。电子显微镜结合二维晶体或单个核糖体的图像重建一直是最有前景的技术,但所得模型的分辨率还不够。在此,我们报告了通过组合4300个冰包埋单颗粒的投影获得的大肠杆菌核糖体25埃分辨率的重建结果。我们的新重建结果揭示了小核糖体亚基中的一个通道和大核糖体亚基中的一个分叉隧道,它们可能分别构成传入信息和新生多肽链的通道。基于这些新发现,提出了蛋白质合成基本框架的三维模型。

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