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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...

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Detalles Bibliográficos
Autores principales: Fritz, Brian R., Jamil, Osman K., Jewett, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
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.
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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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