The Native 3D Organization of Bacterial Polysomes

被引:198
作者
Brandt, Florian [1 ,2 ]
Etchells, Stephanie A. [1 ]
Ortiz, Julio O. [2 ]
Elcock, Adrian H. [4 ]
Hartl, F. Ulrich [1 ,3 ]
Baumeister, Wolfgang [2 ,3 ]
机构
[1] Max Planck Inst Biochem, Dept Cellular Biochem, D-82152 Martinsried, Germany
[2] Max Planck Inst Biochem, Dept Mol Struct Biol, D-82152 Martinsried, Germany
[3] Univ Munich, Ctr Integrated Prot Sci Munich, D-81377 Munich, Germany
[4] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
关键词
COLI 70S RIBOSOME; TRIGGER FACTOR; NASCENT CHAIN; ESCHERICHIA-COLI; MESSENGER-RNA; ELECTRON TOMOGRAPHY; ANGSTROM RESOLUTION; INITIATION-FACTORS; PROTEIN-SYNTHESIS; BINDING-PROTEIN;
D O I
10.1016/j.cell.2008.11.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. coli 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.
引用
收藏
页码:261 / 271
页数:11
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