Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome

被引:90
作者
Abeyrathne, Priyanka D. [1 ]
Koh, Cha San [2 ]
Grant, Timothy [1 ]
Grigorieff, Nikolaus [1 ]
Korostelev, Andrei A. [2 ]
机构
[1] Janelia Res Campus, Howard Hughes Med Inst, Ashburn, VA 20147 USA
[2] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, RNA Therapeut Inst, Worcester, MA USA
来源
ELIFE | 2016年 / 5卷
关键词
ELONGATION-FACTOR-G; CRICKET PARALYSIS VIRUS; MESSENGER-RNA TRANSLOCATION; G-CATALYZED TRANSLOCATION; FUNGAL PROTEIN-SYNTHESIS; ENTRY SITE; INTERNAL RIBOSOME; 70S RIBOSOME; TRANSLATION INITIATION; GTP HYDROLYSIS;
D O I
10.7554/eLife.14874
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Internal ribosome entry sites (IRESs) mediate cap-independent translation of viral mRNAs. Using electron cryo-microscopy of a single specimen, we present five ribosome structures formed with the Taura syndrome virus IRES and translocase eEF2 center dot GTP bound with sordarin. The structures suggest a trajectory of IRES translocation, required for translation initiation, and provide an unprecedented view of eEF2 dynamics. The IRES rearranges from extended to bent to extended conformations. This inchworm-like movement is coupled with ribosomal inter-subunit rotation and 40S head swivel. eEF2, attached to the 60S subunit, slides along the rotating 40S subunit to enter the A site. Its diphthamide-bearing tip at domain IV separates the tRNA-mRNA-like pseudoknot I (PKI) of the IRES from the decoding center. This unlocks 40S domains, facilitating head swivel and biasing IRES translocation via hitherto-elusive intermediates with PKI captured between the A and P sites. The structures suggest missing links in our understanding of tRNA translocation.
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页数:31
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