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Mutational characterization and mapping of the 70S ribosome active site
The synthetic capability of the Escherichia coli ribosome has attracted efforts to repurpose it for novel functions, such as the synthesis of polymers containing non-natural building blocks. However, efforts to repurpose ribosomes are limited by the lack of complete peptidyl transferase center (PTC)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049736/ https://www.ncbi.nlm.nih.gov/pubmed/32009164 http://dx.doi.org/10.1093/nar/gkaa001 |
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author | d’Aquino, Anne E Azim, Tasfia Aleksashin, Nikolay A Hockenberry, Adam J Krüger, Antje Jewett, Michael C |
author_facet | d’Aquino, Anne E Azim, Tasfia Aleksashin, Nikolay A Hockenberry, Adam J Krüger, Antje Jewett, Michael C |
author_sort | d’Aquino, Anne E |
collection | PubMed |
description | The synthetic capability of the Escherichia coli ribosome has attracted efforts to repurpose it for novel functions, such as the synthesis of polymers containing non-natural building blocks. However, efforts to repurpose ribosomes are limited by the lack of complete peptidyl transferase center (PTC) active site mutational analyses to inform design. To address this limitation, we leverage an in vitro ribosome synthesis platform to build and test every possible single nucleotide mutation within the PTC-ring, A-loop and P-loop, 180 total point mutations. These mutant ribosomes were characterized by assessing bulk protein synthesis kinetics, readthrough, assembly, and structure mapping. Despite the highly-conserved nature of the PTC, we found that >85% of the PTC nucleotides possess mutational flexibility. Our work represents a comprehensive single-point mutant characterization and mapping of the 70S ribosome's active site. We anticipate that it will facilitate structure-function relationships within the ribosome and make possible new synthetic biology applications. |
format | Online Article Text |
id | pubmed-7049736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70497362020-03-10 Mutational characterization and mapping of the 70S ribosome active site d’Aquino, Anne E Azim, Tasfia Aleksashin, Nikolay A Hockenberry, Adam J Krüger, Antje Jewett, Michael C Nucleic Acids Res Synthetic Biology and Bioengineering The synthetic capability of the Escherichia coli ribosome has attracted efforts to repurpose it for novel functions, such as the synthesis of polymers containing non-natural building blocks. However, efforts to repurpose ribosomes are limited by the lack of complete peptidyl transferase center (PTC) active site mutational analyses to inform design. To address this limitation, we leverage an in vitro ribosome synthesis platform to build and test every possible single nucleotide mutation within the PTC-ring, A-loop and P-loop, 180 total point mutations. These mutant ribosomes were characterized by assessing bulk protein synthesis kinetics, readthrough, assembly, and structure mapping. Despite the highly-conserved nature of the PTC, we found that >85% of the PTC nucleotides possess mutational flexibility. Our work represents a comprehensive single-point mutant characterization and mapping of the 70S ribosome's active site. We anticipate that it will facilitate structure-function relationships within the ribosome and make possible new synthetic biology applications. Oxford University Press 2020-03-18 2020-02-03 /pmc/articles/PMC7049736/ /pubmed/32009164 http://dx.doi.org/10.1093/nar/gkaa001 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Bioengineering d’Aquino, Anne E Azim, Tasfia Aleksashin, Nikolay A Hockenberry, Adam J Krüger, Antje Jewett, Michael C Mutational characterization and mapping of the 70S ribosome active site |
title | Mutational characterization and mapping of the 70S ribosome active site |
title_full | Mutational characterization and mapping of the 70S ribosome active site |
title_fullStr | Mutational characterization and mapping of the 70S ribosome active site |
title_full_unstemmed | Mutational characterization and mapping of the 70S ribosome active site |
title_short | Mutational characterization and mapping of the 70S ribosome active site |
title_sort | mutational characterization and mapping of the 70s ribosome active site |
topic | Synthetic Biology and Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049736/ https://www.ncbi.nlm.nih.gov/pubmed/32009164 http://dx.doi.org/10.1093/nar/gkaa001 |
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