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Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome
The coupled translocation of transfer RNA and messenger RNA through the ribosome entails large-scale structural rearrangements, including step-wise movements of the tRNAs. Recent structural work has visualized intermediates of translocation induced by elongation factor G (EF-G) with tRNAs trapped in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490557/ https://www.ncbi.nlm.nih.gov/pubmed/26072700 http://dx.doi.org/10.1038/ncomms8442 |
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author | Adio, Sarah Senyushkina, Tamara Peske, Frank Fischer, Niels Wintermeyer, Wolfgang Rodnina, Marina V. |
author_facet | Adio, Sarah Senyushkina, Tamara Peske, Frank Fischer, Niels Wintermeyer, Wolfgang Rodnina, Marina V. |
author_sort | Adio, Sarah |
collection | PubMed |
description | The coupled translocation of transfer RNA and messenger RNA through the ribosome entails large-scale structural rearrangements, including step-wise movements of the tRNAs. Recent structural work has visualized intermediates of translocation induced by elongation factor G (EF-G) with tRNAs trapped in chimeric states with respect to 30S and 50S ribosomal subunits. The functional role of the chimeric states is not known. Here we follow the formation of translocation intermediates by single-molecule fluorescence resonance energy transfer. Using EF-G mutants, a non-hydrolysable GTP analogue, and fusidic acid, we interfere with either translocation or EF-G release from the ribosome and identify several rapidly interconverting chimeric tRNA states on the reaction pathway. EF-G engagement prevents backward transitions early in translocation and increases the fraction of ribosomes that rapidly fluctuate between hybrid, chimeric and posttranslocation states. Thus, the engagement of EF-G alters the energetics of translocation towards a flat energy landscape, thereby promoting forward tRNA movement. |
format | Online Article Text |
id | pubmed-4490557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44905572015-07-13 Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome Adio, Sarah Senyushkina, Tamara Peske, Frank Fischer, Niels Wintermeyer, Wolfgang Rodnina, Marina V. Nat Commun Article The coupled translocation of transfer RNA and messenger RNA through the ribosome entails large-scale structural rearrangements, including step-wise movements of the tRNAs. Recent structural work has visualized intermediates of translocation induced by elongation factor G (EF-G) with tRNAs trapped in chimeric states with respect to 30S and 50S ribosomal subunits. The functional role of the chimeric states is not known. Here we follow the formation of translocation intermediates by single-molecule fluorescence resonance energy transfer. Using EF-G mutants, a non-hydrolysable GTP analogue, and fusidic acid, we interfere with either translocation or EF-G release from the ribosome and identify several rapidly interconverting chimeric tRNA states on the reaction pathway. EF-G engagement prevents backward transitions early in translocation and increases the fraction of ribosomes that rapidly fluctuate between hybrid, chimeric and posttranslocation states. Thus, the engagement of EF-G alters the energetics of translocation towards a flat energy landscape, thereby promoting forward tRNA movement. Nature Pub. Group 2015-06-15 /pmc/articles/PMC4490557/ /pubmed/26072700 http://dx.doi.org/10.1038/ncomms8442 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Adio, Sarah Senyushkina, Tamara Peske, Frank Fischer, Niels Wintermeyer, Wolfgang Rodnina, Marina V. Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome |
title | Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome |
title_full | Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome |
title_fullStr | Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome |
title_full_unstemmed | Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome |
title_short | Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome |
title_sort | fluctuations between multiple ef-g-induced chimeric trna states during translocation on the ribosome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490557/ https://www.ncbi.nlm.nih.gov/pubmed/26072700 http://dx.doi.org/10.1038/ncomms8442 |
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