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Dynamics of Forward and Backward Translocation of mRNA in the Ribosome

Translocation of the mRNA-tRNA complex in the ribosome, which is catalyzed by elongation factor EF-G, is one of critical steps in the elongation cycle of protein synthesis. Besides this conventional forward translocation, the backward translocation can also occur, which can be catalyzed by elongatio...

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Autor principal: Xie, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739767/
https://www.ncbi.nlm.nih.gov/pubmed/23951009
http://dx.doi.org/10.1371/journal.pone.0070789
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author Xie, Ping
author_facet Xie, Ping
author_sort Xie, Ping
collection PubMed
description Translocation of the mRNA-tRNA complex in the ribosome, which is catalyzed by elongation factor EF-G, is one of critical steps in the elongation cycle of protein synthesis. Besides this conventional forward translocation, the backward translocation can also occur, which can be catalyzed by elongation factor LepA. However, the molecular mechanism of the translocation remains elusive. To understand the mechanism, here we study theoretically the dynamics of the forward translocation under various nucleotide states of EF-G and the backward translocation in the absence of and in the presence of LepA. We present a consistent explanation of spontaneous forward translocations in the absence of EF-G, the EF-G-catalyzed forward translocations in the presence of a non-hydrolysable GTP analogue and in the presence of GTP, and the spontaneous and LepA-catalyzed backward translocation. The theoretical results provide quantitative explanations of a lot of different, independent experimental data, and also provide testable predictions.
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spelling pubmed-37397672013-08-15 Dynamics of Forward and Backward Translocation of mRNA in the Ribosome Xie, Ping PLoS One Research Article Translocation of the mRNA-tRNA complex in the ribosome, which is catalyzed by elongation factor EF-G, is one of critical steps in the elongation cycle of protein synthesis. Besides this conventional forward translocation, the backward translocation can also occur, which can be catalyzed by elongation factor LepA. However, the molecular mechanism of the translocation remains elusive. To understand the mechanism, here we study theoretically the dynamics of the forward translocation under various nucleotide states of EF-G and the backward translocation in the absence of and in the presence of LepA. We present a consistent explanation of spontaneous forward translocations in the absence of EF-G, the EF-G-catalyzed forward translocations in the presence of a non-hydrolysable GTP analogue and in the presence of GTP, and the spontaneous and LepA-catalyzed backward translocation. The theoretical results provide quantitative explanations of a lot of different, independent experimental data, and also provide testable predictions. Public Library of Science 2013-08-09 /pmc/articles/PMC3739767/ /pubmed/23951009 http://dx.doi.org/10.1371/journal.pone.0070789 Text en © 2013 Ping Xie http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xie, Ping
Dynamics of Forward and Backward Translocation of mRNA in the Ribosome
title Dynamics of Forward and Backward Translocation of mRNA in the Ribosome
title_full Dynamics of Forward and Backward Translocation of mRNA in the Ribosome
title_fullStr Dynamics of Forward and Backward Translocation of mRNA in the Ribosome
title_full_unstemmed Dynamics of Forward and Backward Translocation of mRNA in the Ribosome
title_short Dynamics of Forward and Backward Translocation of mRNA in the Ribosome
title_sort dynamics of forward and backward translocation of mrna in the ribosome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739767/
https://www.ncbi.nlm.nih.gov/pubmed/23951009
http://dx.doi.org/10.1371/journal.pone.0070789
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