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De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation

Intercellular signaling is indispensable for single cells to form complex biological structures, such as biofilms, tissues and organs. The genetic tools available for engineering intercellular signaling, however, are quite limited. Here we exploit the chemical diversity of biological small molecules...

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Autores principales: Du, Pei, Zhao, Huiwei, Zhang, Haoqian, Wang, Ruisha, Huang, Jianyi, Tian, Ye, Luo, Xudong, Luo, Xunxun, Wang, Min, Xiang, Yanhui, Qian, Long, Chen, Yihua, Tao, Yong, Lou, Chunbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445162/
https://www.ncbi.nlm.nih.gov/pubmed/32839450
http://dx.doi.org/10.1038/s41467-020-17993-w
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author Du, Pei
Zhao, Huiwei
Zhang, Haoqian
Wang, Ruisha
Huang, Jianyi
Tian, Ye
Luo, Xudong
Luo, Xunxun
Wang, Min
Xiang, Yanhui
Qian, Long
Chen, Yihua
Tao, Yong
Lou, Chunbo
author_facet Du, Pei
Zhao, Huiwei
Zhang, Haoqian
Wang, Ruisha
Huang, Jianyi
Tian, Ye
Luo, Xudong
Luo, Xunxun
Wang, Min
Xiang, Yanhui
Qian, Long
Chen, Yihua
Tao, Yong
Lou, Chunbo
author_sort Du, Pei
collection PubMed
description Intercellular signaling is indispensable for single cells to form complex biological structures, such as biofilms, tissues and organs. The genetic tools available for engineering intercellular signaling, however, are quite limited. Here we exploit the chemical diversity of biological small molecules to de novo design a genetic toolbox for high-performance, multi-channel cell–cell communications and biological computations. By biosynthetic pathway design for signal molecules, rational engineering of sensing promoters and directed evolution of sensing transcription factors, we obtain six cell–cell signaling channels in bacteria with orthogonality far exceeding the conventional quorum sensing systems and successfully transfer some of them into yeast and human cells. For demonstration, they are applied in cell consortia to generate bacterial colony-patterns using up to four signaling channels simultaneously and to implement distributed bio-computation containing seven different strains as basic units. This intercellular signaling toolbox paves the way for engineering complex multicellularity including artificial ecosystems and smart tissues.
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spelling pubmed-74451622020-09-02 De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation Du, Pei Zhao, Huiwei Zhang, Haoqian Wang, Ruisha Huang, Jianyi Tian, Ye Luo, Xudong Luo, Xunxun Wang, Min Xiang, Yanhui Qian, Long Chen, Yihua Tao, Yong Lou, Chunbo Nat Commun Article Intercellular signaling is indispensable for single cells to form complex biological structures, such as biofilms, tissues and organs. The genetic tools available for engineering intercellular signaling, however, are quite limited. Here we exploit the chemical diversity of biological small molecules to de novo design a genetic toolbox for high-performance, multi-channel cell–cell communications and biological computations. By biosynthetic pathway design for signal molecules, rational engineering of sensing promoters and directed evolution of sensing transcription factors, we obtain six cell–cell signaling channels in bacteria with orthogonality far exceeding the conventional quorum sensing systems and successfully transfer some of them into yeast and human cells. For demonstration, they are applied in cell consortia to generate bacterial colony-patterns using up to four signaling channels simultaneously and to implement distributed bio-computation containing seven different strains as basic units. This intercellular signaling toolbox paves the way for engineering complex multicellularity including artificial ecosystems and smart tissues. Nature Publishing Group UK 2020-08-24 /pmc/articles/PMC7445162/ /pubmed/32839450 http://dx.doi.org/10.1038/s41467-020-17993-w Text en © The Author(s) 2020 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
Du, Pei
Zhao, Huiwei
Zhang, Haoqian
Wang, Ruisha
Huang, Jianyi
Tian, Ye
Luo, Xudong
Luo, Xunxun
Wang, Min
Xiang, Yanhui
Qian, Long
Chen, Yihua
Tao, Yong
Lou, Chunbo
De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
title De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
title_full De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
title_fullStr De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
title_full_unstemmed De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
title_short De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
title_sort de novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445162/
https://www.ncbi.nlm.nih.gov/pubmed/32839450
http://dx.doi.org/10.1038/s41467-020-17993-w
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