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Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction
In vitro construction of Escherichia coli ribosomes could elucidate a deeper understanding of these complex molecular machines and make possible the production of synthetic variants with new functions. Toward this goal, we recently developed an integrated synthesis, assembly and translation (iSAT) s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482083/ https://www.ncbi.nlm.nih.gov/pubmed/25897121 http://dx.doi.org/10.1093/nar/gkv329 |
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author | Fritz, Brian R. Jamil, Osman K. Jewett, Michael C. |
author_facet | Fritz, Brian R. Jamil, Osman K. Jewett, Michael C. |
author_sort | Fritz, Brian R. |
collection | PubMed |
description | In vitro construction of Escherichia coli ribosomes could elucidate a deeper understanding of these complex molecular machines and make possible the production of synthetic variants with new functions. Toward this goal, we recently developed an integrated synthesis, assembly and translation (iSAT) system that allows for co-activation of ribosomal RNA (rRNA) transcription and ribosome assembly, mRNA transcription and protein translation without intact cells. Here, we discovered that macromolecular crowding and reducing agents increase overall iSAT protein synthesis; the combination of 6% w/v Ficoll 400 and 2 mM DTBA yielded approximately a five-fold increase in overall iSAT protein synthesis activity. By utilizing a fluorescent RNA aptamer, fluorescent reporter proteins and ribosome sedimentation analysis, we showed that crowding agents increase iSAT yields by enhancing translation while reducing agents increase rRNA transcription and ribosome assembly. Finally, we showed that iSAT ribosomes possess ∼70% of the protein synthesis activity of in vivo-assembled E. coli ribosomes. This work improves iSAT protein synthesis through the addition of crowding and reducing agents, provides a thorough understanding of the effect of these additives within the iSAT system and demonstrates how iSAT allows for manipulation and analysis of ribosome biogenesis in the context of an in vitro transcription-translation system. |
format | Online Article Text |
id | pubmed-4482083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44820832015-06-30 Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction Fritz, Brian R. Jamil, Osman K. Jewett, Michael C. Nucleic Acids Res Synthetic Biology and Bioengineering In vitro construction of Escherichia coli ribosomes could elucidate a deeper understanding of these complex molecular machines and make possible the production of synthetic variants with new functions. Toward this goal, we recently developed an integrated synthesis, assembly and translation (iSAT) system that allows for co-activation of ribosomal RNA (rRNA) transcription and ribosome assembly, mRNA transcription and protein translation without intact cells. Here, we discovered that macromolecular crowding and reducing agents increase overall iSAT protein synthesis; the combination of 6% w/v Ficoll 400 and 2 mM DTBA yielded approximately a five-fold increase in overall iSAT protein synthesis activity. By utilizing a fluorescent RNA aptamer, fluorescent reporter proteins and ribosome sedimentation analysis, we showed that crowding agents increase iSAT yields by enhancing translation while reducing agents increase rRNA transcription and ribosome assembly. Finally, we showed that iSAT ribosomes possess ∼70% of the protein synthesis activity of in vivo-assembled E. coli ribosomes. This work improves iSAT protein synthesis through the addition of crowding and reducing agents, provides a thorough understanding of the effect of these additives within the iSAT system and demonstrates how iSAT allows for manipulation and analysis of ribosome biogenesis in the context of an in vitro transcription-translation system. Oxford University Press 2015-05-19 2015-04-20 /pmc/articles/PMC4482083/ /pubmed/25897121 http://dx.doi.org/10.1093/nar/gkv329 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Synthetic Biology and Bioengineering Fritz, Brian R. Jamil, Osman K. Jewett, Michael C. Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
title | Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
title_full | Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
title_fullStr | Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
title_full_unstemmed | Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
title_short | Implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
title_sort | implications of macromolecular crowding and reducing conditions for in vitro ribosome construction |
topic | Synthetic Biology and Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482083/ https://www.ncbi.nlm.nih.gov/pubmed/25897121 http://dx.doi.org/10.1093/nar/gkv329 |
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