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Engineered ribosomes with tethered subunits for expanding biological function
Ribo-T is a ribosome with covalently tethered subunits where core 16S and 23S ribosomal RNAs form a single chimeric molecule. Ribo-T makes possible a functionally orthogonal ribosome–mRNA system in cells. Unfortunately, use of Ribo-T has been limited because of low activity of its original version....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718428/ https://www.ncbi.nlm.nih.gov/pubmed/31477696 http://dx.doi.org/10.1038/s41467-019-11427-y |
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author | Carlson, Erik D. d’Aquino, Anne E. Kim, Do Soon Fulk, Emily M. Hoang, Kim Szal, Teresa Mankin, Alexander S. Jewett, Michael C. |
author_facet | Carlson, Erik D. d’Aquino, Anne E. Kim, Do Soon Fulk, Emily M. Hoang, Kim Szal, Teresa Mankin, Alexander S. Jewett, Michael C. |
author_sort | Carlson, Erik D. |
collection | PubMed |
description | Ribo-T is a ribosome with covalently tethered subunits where core 16S and 23S ribosomal RNAs form a single chimeric molecule. Ribo-T makes possible a functionally orthogonal ribosome–mRNA system in cells. Unfortunately, use of Ribo-T has been limited because of low activity of its original version. Here, to overcome this limitation, we use an evolutionary approach to select new tether designs that are capable of supporting faster cell growth and increased protein expression. Further, we evolve new orthogonal Ribo-T/mRNA pairs that function in parallel with, but independent of, natural ribosomes and mRNAs, increasing the efficiency of orthogonal protein expression. The Ribo-T with optimized designs is able to synthesize a diverse set of proteins, and can also incorporate multiple non-canonical amino acids into synthesized polypeptides. The enhanced Ribo-T designs should be useful for exploring poorly understood functions of the ribosome and engineering ribosomes with altered catalytic properties. |
format | Online Article Text |
id | pubmed-6718428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67184282019-09-04 Engineered ribosomes with tethered subunits for expanding biological function Carlson, Erik D. d’Aquino, Anne E. Kim, Do Soon Fulk, Emily M. Hoang, Kim Szal, Teresa Mankin, Alexander S. Jewett, Michael C. Nat Commun Article Ribo-T is a ribosome with covalently tethered subunits where core 16S and 23S ribosomal RNAs form a single chimeric molecule. Ribo-T makes possible a functionally orthogonal ribosome–mRNA system in cells. Unfortunately, use of Ribo-T has been limited because of low activity of its original version. Here, to overcome this limitation, we use an evolutionary approach to select new tether designs that are capable of supporting faster cell growth and increased protein expression. Further, we evolve new orthogonal Ribo-T/mRNA pairs that function in parallel with, but independent of, natural ribosomes and mRNAs, increasing the efficiency of orthogonal protein expression. The Ribo-T with optimized designs is able to synthesize a diverse set of proteins, and can also incorporate multiple non-canonical amino acids into synthesized polypeptides. The enhanced Ribo-T designs should be useful for exploring poorly understood functions of the ribosome and engineering ribosomes with altered catalytic properties. Nature Publishing Group UK 2019-09-02 /pmc/articles/PMC6718428/ /pubmed/31477696 http://dx.doi.org/10.1038/s41467-019-11427-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Carlson, Erik D. d’Aquino, Anne E. Kim, Do Soon Fulk, Emily M. Hoang, Kim Szal, Teresa Mankin, Alexander S. Jewett, Michael C. Engineered ribosomes with tethered subunits for expanding biological function |
title | Engineered ribosomes with tethered subunits for expanding biological function |
title_full | Engineered ribosomes with tethered subunits for expanding biological function |
title_fullStr | Engineered ribosomes with tethered subunits for expanding biological function |
title_full_unstemmed | Engineered ribosomes with tethered subunits for expanding biological function |
title_short | Engineered ribosomes with tethered subunits for expanding biological function |
title_sort | engineered ribosomes with tethered subunits for expanding biological function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718428/ https://www.ncbi.nlm.nih.gov/pubmed/31477696 http://dx.doi.org/10.1038/s41467-019-11427-y |
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