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Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation

Many antibiotics that bind to the ribosome inhibit translation by blocking the movement of tRNAs and mRNA or interfering with ribosome dynamics, which impairs the formation of essential translocation intermediates. Here we show how translocation inhibitors viomycin (Vio), neomycin (Neo), paromomycin...

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Autores principales: Belardinelli, Riccardo, Sharma, Heena, Peske, Frank, Rodnina, Marina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370747/
https://www.ncbi.nlm.nih.gov/pubmed/34117118
http://dx.doi.org/10.1261/rna.078758.121
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author Belardinelli, Riccardo
Sharma, Heena
Peske, Frank
Rodnina, Marina V.
author_facet Belardinelli, Riccardo
Sharma, Heena
Peske, Frank
Rodnina, Marina V.
author_sort Belardinelli, Riccardo
collection PubMed
description Many antibiotics that bind to the ribosome inhibit translation by blocking the movement of tRNAs and mRNA or interfering with ribosome dynamics, which impairs the formation of essential translocation intermediates. Here we show how translocation inhibitors viomycin (Vio), neomycin (Neo), paromomycin (Par), kanamycin (Kan), spectinomycin (Spc), hygromycin B (HygB), and streptomycin (Str, an antibiotic that does not inhibit tRNA movement), affect principal motions of the small ribosomal subunits (SSU) during EF-G-promoted translocation. Using ensemble kinetics, we studied the SSU body domain rotation and SSU head domain swiveling in real time. We show that although antibiotics binding to the ribosome can favor a particular ribosome conformation in the absence of EF-G, their kinetic effect on the EF-G-induced transition to the rotated/swiveled state of the SSU is moderate. The antibiotics mostly inhibit backward movements of the SSU body and/or the head domains. Vio, Spc, and high concentrations of Neo completely inhibit the backward movements of the SSU body and head domain. Kan, Par, HygB, and low concentrations of Neo slow down both movements, but their sequence and coordination are retained. Finally, Str has very little effect on the backward rotation of the SSU body domain, but retards the SSU head movement. The data underscore the importance of ribosome dynamics for tRNA-mRNA translocation and provide new insights into the mechanism of antibiotic action.
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spelling pubmed-83707472021-09-01 Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation Belardinelli, Riccardo Sharma, Heena Peske, Frank Rodnina, Marina V. RNA Article Many antibiotics that bind to the ribosome inhibit translation by blocking the movement of tRNAs and mRNA or interfering with ribosome dynamics, which impairs the formation of essential translocation intermediates. Here we show how translocation inhibitors viomycin (Vio), neomycin (Neo), paromomycin (Par), kanamycin (Kan), spectinomycin (Spc), hygromycin B (HygB), and streptomycin (Str, an antibiotic that does not inhibit tRNA movement), affect principal motions of the small ribosomal subunits (SSU) during EF-G-promoted translocation. Using ensemble kinetics, we studied the SSU body domain rotation and SSU head domain swiveling in real time. We show that although antibiotics binding to the ribosome can favor a particular ribosome conformation in the absence of EF-G, their kinetic effect on the EF-G-induced transition to the rotated/swiveled state of the SSU is moderate. The antibiotics mostly inhibit backward movements of the SSU body and/or the head domains. Vio, Spc, and high concentrations of Neo completely inhibit the backward movements of the SSU body and head domain. Kan, Par, HygB, and low concentrations of Neo slow down both movements, but their sequence and coordination are retained. Finally, Str has very little effect on the backward rotation of the SSU body domain, but retards the SSU head movement. The data underscore the importance of ribosome dynamics for tRNA-mRNA translocation and provide new insights into the mechanism of antibiotic action. Cold Spring Harbor Laboratory Press 2021-09 /pmc/articles/PMC8370747/ /pubmed/34117118 http://dx.doi.org/10.1261/rna.078758.121 Text en © 2021 Belardinelli et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Article
Belardinelli, Riccardo
Sharma, Heena
Peske, Frank
Rodnina, Marina V.
Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation
title Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation
title_full Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation
title_fullStr Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation
title_full_unstemmed Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation
title_short Perturbation of ribosomal subunit dynamics by inhibitors of tRNA translocation
title_sort perturbation of ribosomal subunit dynamics by inhibitors of trna translocation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370747/
https://www.ncbi.nlm.nih.gov/pubmed/34117118
http://dx.doi.org/10.1261/rna.078758.121
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