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A scalable peptide-GPCR language for engineering multicellular communication
Engineering multicellularity is one of the next breakthroughs for Synthetic Biology. A key bottleneck to building multicellular systems is the lack of a scalable signaling language with a large number of interfaces that can be used simultaneously. Here, we present a modular, scalable, intercellular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265332/ https://www.ncbi.nlm.nih.gov/pubmed/30498215 http://dx.doi.org/10.1038/s41467-018-07610-2 |
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author | Billerbeck, Sonja Brisbois, James Agmon, Neta Jimenez, Miguel Temple, Jasmine Shen, Michael Boeke, Jef D. Cornish, Virginia W. |
author_facet | Billerbeck, Sonja Brisbois, James Agmon, Neta Jimenez, Miguel Temple, Jasmine Shen, Michael Boeke, Jef D. Cornish, Virginia W. |
author_sort | Billerbeck, Sonja |
collection | PubMed |
description | Engineering multicellularity is one of the next breakthroughs for Synthetic Biology. A key bottleneck to building multicellular systems is the lack of a scalable signaling language with a large number of interfaces that can be used simultaneously. Here, we present a modular, scalable, intercellular signaling language in yeast based on fungal mating peptide/G-protein-coupled receptor (GPCR) pairs harnessed from nature. First, through genome-mining, we assemble 32 functional peptide-GPCR signaling interfaces with a range of dose-response characteristics. Next, we demonstrate that these interfaces can be combined into two-cell communication links, which serve as assembly units for higher-order communication topologies. Finally, we show 56 functional, two-cell links, which we use to assemble three- to six-member communication topologies and a three-member interdependent community. Importantly, our peptide-GPCR language is scalable and tunable by genetic encoding, requires minimal component engineering, and should be massively scalable by further application of our genome mining pipeline or directed evolution. |
format | Online Article Text |
id | pubmed-6265332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62653322018-12-03 A scalable peptide-GPCR language for engineering multicellular communication Billerbeck, Sonja Brisbois, James Agmon, Neta Jimenez, Miguel Temple, Jasmine Shen, Michael Boeke, Jef D. Cornish, Virginia W. Nat Commun Article Engineering multicellularity is one of the next breakthroughs for Synthetic Biology. A key bottleneck to building multicellular systems is the lack of a scalable signaling language with a large number of interfaces that can be used simultaneously. Here, we present a modular, scalable, intercellular signaling language in yeast based on fungal mating peptide/G-protein-coupled receptor (GPCR) pairs harnessed from nature. First, through genome-mining, we assemble 32 functional peptide-GPCR signaling interfaces with a range of dose-response characteristics. Next, we demonstrate that these interfaces can be combined into two-cell communication links, which serve as assembly units for higher-order communication topologies. Finally, we show 56 functional, two-cell links, which we use to assemble three- to six-member communication topologies and a three-member interdependent community. Importantly, our peptide-GPCR language is scalable and tunable by genetic encoding, requires minimal component engineering, and should be massively scalable by further application of our genome mining pipeline or directed evolution. Nature Publishing Group UK 2018-11-29 /pmc/articles/PMC6265332/ /pubmed/30498215 http://dx.doi.org/10.1038/s41467-018-07610-2 Text en © The Author(s) 2018 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 Billerbeck, Sonja Brisbois, James Agmon, Neta Jimenez, Miguel Temple, Jasmine Shen, Michael Boeke, Jef D. Cornish, Virginia W. A scalable peptide-GPCR language for engineering multicellular communication |
title | A scalable peptide-GPCR language for engineering multicellular communication |
title_full | A scalable peptide-GPCR language for engineering multicellular communication |
title_fullStr | A scalable peptide-GPCR language for engineering multicellular communication |
title_full_unstemmed | A scalable peptide-GPCR language for engineering multicellular communication |
title_short | A scalable peptide-GPCR language for engineering multicellular communication |
title_sort | scalable peptide-gpcr language for engineering multicellular communication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265332/ https://www.ncbi.nlm.nih.gov/pubmed/30498215 http://dx.doi.org/10.1038/s41467-018-07610-2 |
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