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Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation

In bacterial translational initiation, three initiation factors (IFs 1–3) enable the selection of initiator tRNA and the start codon in the P site of the 30S ribosomal subunit. Here, we report 11 single-particle cryo-electron microscopy (cryoEM) reconstructions of the complex of bacterial 30S subuni...

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Autores principales: Hussain, Tanweer, Llácer, Jose L., Wimberly, Brian T., Kieft, Jeffrey S., Ramakrishnan, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037330/
https://www.ncbi.nlm.nih.gov/pubmed/27662086
http://dx.doi.org/10.1016/j.cell.2016.08.074
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author Hussain, Tanweer
Llácer, Jose L.
Wimberly, Brian T.
Kieft, Jeffrey S.
Ramakrishnan, V.
author_facet Hussain, Tanweer
Llácer, Jose L.
Wimberly, Brian T.
Kieft, Jeffrey S.
Ramakrishnan, V.
author_sort Hussain, Tanweer
collection PubMed
description In bacterial translational initiation, three initiation factors (IFs 1–3) enable the selection of initiator tRNA and the start codon in the P site of the 30S ribosomal subunit. Here, we report 11 single-particle cryo-electron microscopy (cryoEM) reconstructions of the complex of bacterial 30S subunit with initiator tRNA, mRNA, and IFs 1–3, representing different steps along the initiation pathway. IF1 provides key anchoring points for IF2 and IF3, thereby enhancing their activities. IF2 positions a domain in an extended conformation appropriate for capturing the formylmethionyl moiety charged on tRNA. IF3 and tRNA undergo large conformational changes to facilitate the accommodation of the formylmethionyl-tRNA (fMet-tRNA(fMet)) into the P site for start codon recognition.
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spelling pubmed-50373302016-09-30 Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation Hussain, Tanweer Llácer, Jose L. Wimberly, Brian T. Kieft, Jeffrey S. Ramakrishnan, V. Cell Article In bacterial translational initiation, three initiation factors (IFs 1–3) enable the selection of initiator tRNA and the start codon in the P site of the 30S ribosomal subunit. Here, we report 11 single-particle cryo-electron microscopy (cryoEM) reconstructions of the complex of bacterial 30S subunit with initiator tRNA, mRNA, and IFs 1–3, representing different steps along the initiation pathway. IF1 provides key anchoring points for IF2 and IF3, thereby enhancing their activities. IF2 positions a domain in an extended conformation appropriate for capturing the formylmethionyl moiety charged on tRNA. IF3 and tRNA undergo large conformational changes to facilitate the accommodation of the formylmethionyl-tRNA (fMet-tRNA(fMet)) into the P site for start codon recognition. Cell Press 2016-09-22 /pmc/articles/PMC5037330/ /pubmed/27662086 http://dx.doi.org/10.1016/j.cell.2016.08.074 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hussain, Tanweer
Llácer, Jose L.
Wimberly, Brian T.
Kieft, Jeffrey S.
Ramakrishnan, V.
Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation
title Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation
title_full Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation
title_fullStr Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation
title_full_unstemmed Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation
title_short Large-Scale Movements of IF3 and tRNA during Bacterial Translation Initiation
title_sort large-scale movements of if3 and trna during bacterial translation initiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037330/
https://www.ncbi.nlm.nih.gov/pubmed/27662086
http://dx.doi.org/10.1016/j.cell.2016.08.074
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