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Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome
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•GTP bound with sordarin. The structures suggest a trajecto...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896748/ https://www.ncbi.nlm.nih.gov/pubmed/27159452 http://dx.doi.org/10.7554/eLife.14874 |
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author | Abeyrathne, Priyanka D Koh, Cha San Grant, Timothy Grigorieff, Nikolaus Korostelev, Andrei A |
author_facet | Abeyrathne, Priyanka D Koh, Cha San Grant, Timothy Grigorieff, Nikolaus Korostelev, Andrei A |
author_sort | Abeyrathne, Priyanka D |
collection | PubMed |
description | 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•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. DOI: http://dx.doi.org/10.7554/eLife.14874.001 |
format | Online Article Text |
id | pubmed-4896748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48967482016-06-08 Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome Abeyrathne, Priyanka D Koh, Cha San Grant, Timothy Grigorieff, Nikolaus Korostelev, Andrei A eLife Biochemistry 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•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. DOI: http://dx.doi.org/10.7554/eLife.14874.001 eLife Sciences Publications, Ltd 2016-05-09 /pmc/articles/PMC4896748/ /pubmed/27159452 http://dx.doi.org/10.7554/eLife.14874 Text en © 2016, Abeyrathne et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Abeyrathne, Priyanka D Koh, Cha San Grant, Timothy Grigorieff, Nikolaus Korostelev, Andrei A Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome |
title | Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome |
title_full | Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome |
title_fullStr | Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome |
title_full_unstemmed | Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome |
title_short | Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome |
title_sort | ensemble cryo-em uncovers inchworm-like translocation of a viral ires through the ribosome |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896748/ https://www.ncbi.nlm.nih.gov/pubmed/27159452 http://dx.doi.org/10.7554/eLife.14874 |
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