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Ribosome Assembly as Antimicrobial Target

Many antibiotics target the ribosome and interfere with its translation cycle. Since translation is the source of all cellular proteins including ribosomal proteins, protein synthesis and ribosome assembly are interdependent. As a consequence, the activity of translation inhibitors might indirectly...

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Detalles Bibliográficos
Autores principales: Nikolay, Rainer, Schmidt, Sabine, Schlömer, Renate, Deuerling, Elke, Nierhaus, Knud H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929433/
https://www.ncbi.nlm.nih.gov/pubmed/27240412
http://dx.doi.org/10.3390/antibiotics5020018
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author Nikolay, Rainer
Schmidt, Sabine
Schlömer, Renate
Deuerling, Elke
Nierhaus, Knud H.
author_facet Nikolay, Rainer
Schmidt, Sabine
Schlömer, Renate
Deuerling, Elke
Nierhaus, Knud H.
author_sort Nikolay, Rainer
collection PubMed
description Many antibiotics target the ribosome and interfere with its translation cycle. Since translation is the source of all cellular proteins including ribosomal proteins, protein synthesis and ribosome assembly are interdependent. As a consequence, the activity of translation inhibitors might indirectly cause defective ribosome assembly. Due to the difficulty in distinguishing between direct and indirect effects, and because assembly is probably a target in its own right, concepts are needed to identify small molecules that directly inhibit ribosome assembly. Here, we summarize the basic facts of ribosome targeting antibiotics. Furthermore, we present an in vivo screening strategy that focuses on ribosome assembly by a direct fluorescence based read-out that aims to identify and characterize small molecules acting as primary assembly inhibitors.
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spelling pubmed-49294332016-07-07 Ribosome Assembly as Antimicrobial Target Nikolay, Rainer Schmidt, Sabine Schlömer, Renate Deuerling, Elke Nierhaus, Knud H. Antibiotics (Basel) Article Many antibiotics target the ribosome and interfere with its translation cycle. Since translation is the source of all cellular proteins including ribosomal proteins, protein synthesis and ribosome assembly are interdependent. As a consequence, the activity of translation inhibitors might indirectly cause defective ribosome assembly. Due to the difficulty in distinguishing between direct and indirect effects, and because assembly is probably a target in its own right, concepts are needed to identify small molecules that directly inhibit ribosome assembly. Here, we summarize the basic facts of ribosome targeting antibiotics. Furthermore, we present an in vivo screening strategy that focuses on ribosome assembly by a direct fluorescence based read-out that aims to identify and characterize small molecules acting as primary assembly inhibitors. MDPI 2016-05-27 /pmc/articles/PMC4929433/ /pubmed/27240412 http://dx.doi.org/10.3390/antibiotics5020018 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nikolay, Rainer
Schmidt, Sabine
Schlömer, Renate
Deuerling, Elke
Nierhaus, Knud H.
Ribosome Assembly as Antimicrobial Target
title Ribosome Assembly as Antimicrobial Target
title_full Ribosome Assembly as Antimicrobial Target
title_fullStr Ribosome Assembly as Antimicrobial Target
title_full_unstemmed Ribosome Assembly as Antimicrobial Target
title_short Ribosome Assembly as Antimicrobial Target
title_sort ribosome assembly as antimicrobial target
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929433/
https://www.ncbi.nlm.nih.gov/pubmed/27240412
http://dx.doi.org/10.3390/antibiotics5020018
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