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Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions
Engineered living materials (ELMs) are gaining traction among synthetic biologists, as their emergent properties and nonequilibrium thermodynamics make them markedly different from traditional materials. However, the aspiration to directly use living cells as building blocks to create higher-order s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635822/ https://www.ncbi.nlm.nih.gov/pubmed/36332017 http://dx.doi.org/10.1126/sciadv.ade0073 |
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author | Yi, Qikun Dai, Xin Park, Byung Min Gu, Junhao Luo, Jiren Wang, Ri Yu, Cong Kou, Songzi Huang, Jinqing Lakerveld, Richard Sun, Fei |
author_facet | Yi, Qikun Dai, Xin Park, Byung Min Gu, Junhao Luo, Jiren Wang, Ri Yu, Cong Kou, Songzi Huang, Jinqing Lakerveld, Richard Sun, Fei |
author_sort | Yi, Qikun |
collection | PubMed |
description | Engineered living materials (ELMs) are gaining traction among synthetic biologists, as their emergent properties and nonequilibrium thermodynamics make them markedly different from traditional materials. However, the aspiration to directly use living cells as building blocks to create higher-order structures or materials, with no need for chemical modification, remains elusive to synthetic biologists. Here, we report a strategy that enables the assembly of engineered Saccharomyces cerevisiae into self-propagating ELMs via ultrahigh-affinity protein/protein interactions. These yeast cells have been genetically engineered to display the protein pairs SpyTag/SpyCatcher or CL7/Im7 on their surfaces, which enable their assembly into multicellular structures capable of further growth and proliferation. The assembly process can be controlled precisely via optical tweezers or microfluidics. Moreover, incorporation of functional motifs such as super uranyl-binding protein and mussel foot proteins via genetic programming rendered these materials suitable for uranium extraction from seawater and bioadhesion, respectively, pointing to their potential in chemical separation and biomedical applications. |
format | Online Article Text |
id | pubmed-9635822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96358222022-11-18 Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions Yi, Qikun Dai, Xin Park, Byung Min Gu, Junhao Luo, Jiren Wang, Ri Yu, Cong Kou, Songzi Huang, Jinqing Lakerveld, Richard Sun, Fei Sci Adv Biomedicine and Life Sciences Engineered living materials (ELMs) are gaining traction among synthetic biologists, as their emergent properties and nonequilibrium thermodynamics make them markedly different from traditional materials. However, the aspiration to directly use living cells as building blocks to create higher-order structures or materials, with no need for chemical modification, remains elusive to synthetic biologists. Here, we report a strategy that enables the assembly of engineered Saccharomyces cerevisiae into self-propagating ELMs via ultrahigh-affinity protein/protein interactions. These yeast cells have been genetically engineered to display the protein pairs SpyTag/SpyCatcher or CL7/Im7 on their surfaces, which enable their assembly into multicellular structures capable of further growth and proliferation. The assembly process can be controlled precisely via optical tweezers or microfluidics. Moreover, incorporation of functional motifs such as super uranyl-binding protein and mussel foot proteins via genetic programming rendered these materials suitable for uranium extraction from seawater and bioadhesion, respectively, pointing to their potential in chemical separation and biomedical applications. American Association for the Advancement of Science 2022-11-04 /pmc/articles/PMC9635822/ /pubmed/36332017 http://dx.doi.org/10.1126/sciadv.ade0073 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Yi, Qikun Dai, Xin Park, Byung Min Gu, Junhao Luo, Jiren Wang, Ri Yu, Cong Kou, Songzi Huang, Jinqing Lakerveld, Richard Sun, Fei Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
title | Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
title_full | Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
title_fullStr | Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
title_full_unstemmed | Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
title_short | Directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
title_sort | directed assembly of genetically engineered eukaryotic cells into living functional materials via ultrahigh-affinity protein interactions |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635822/ https://www.ncbi.nlm.nih.gov/pubmed/36332017 http://dx.doi.org/10.1126/sciadv.ade0073 |
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