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Exploiting spatial dimensions to enable parallelized continuous directed evolution
Current strategies to improve the throughput of continuous directed evolution technologies often involve complex mechanical fluid‐controlling system or robotic platforms, which limits their popularization and application in general laboratories. Inspired by our previous study on bacterial range expa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491160/ https://www.ncbi.nlm.nih.gov/pubmed/36129229 http://dx.doi.org/10.15252/msb.202210934 |
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author | Wei, Ting Lai, Wangsheng Chen, Qian Zhang, Yi Sun, Chenjian He, Xionglei Zhao, Guoping Fu, Xiongfei Liu, Chenli |
author_facet | Wei, Ting Lai, Wangsheng Chen, Qian Zhang, Yi Sun, Chenjian He, Xionglei Zhao, Guoping Fu, Xiongfei Liu, Chenli |
author_sort | Wei, Ting |
collection | PubMed |
description | Current strategies to improve the throughput of continuous directed evolution technologies often involve complex mechanical fluid‐controlling system or robotic platforms, which limits their popularization and application in general laboratories. Inspired by our previous study on bacterial range expansion, in this study, we report a system termed SPACE for rapid and extensively parallelizable evolution of biomolecules by introducing spatial dimensions into the landmark phage‐assisted continuous evolution system. Specifically, M13 phages and chemotactic Escherichia coli cells were closely inoculated onto a semisolid agar. The phages came into contact with the expanding front of the bacterial range, and then comigrated with the bacteria. This system leverages competition over space, wherein evolutionary progress is closely associated with the production of spatial patterns, allowing the emergence of improved or new protein functions. In a prototypical problem, SPACE remarkably simplified the process and evolved the promoter recognition of T7 RNA polymerase (RNAP) to a library of 96 random sequences in parallel. These results establish SPACE as a simple, easy to implement, and massively parallelizable platform for continuous directed evolution in general laboratories. |
format | Online Article Text |
id | pubmed-9491160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94911602022-09-30 Exploiting spatial dimensions to enable parallelized continuous directed evolution Wei, Ting Lai, Wangsheng Chen, Qian Zhang, Yi Sun, Chenjian He, Xionglei Zhao, Guoping Fu, Xiongfei Liu, Chenli Mol Syst Biol Articles Current strategies to improve the throughput of continuous directed evolution technologies often involve complex mechanical fluid‐controlling system or robotic platforms, which limits their popularization and application in general laboratories. Inspired by our previous study on bacterial range expansion, in this study, we report a system termed SPACE for rapid and extensively parallelizable evolution of biomolecules by introducing spatial dimensions into the landmark phage‐assisted continuous evolution system. Specifically, M13 phages and chemotactic Escherichia coli cells were closely inoculated onto a semisolid agar. The phages came into contact with the expanding front of the bacterial range, and then comigrated with the bacteria. This system leverages competition over space, wherein evolutionary progress is closely associated with the production of spatial patterns, allowing the emergence of improved or new protein functions. In a prototypical problem, SPACE remarkably simplified the process and evolved the promoter recognition of T7 RNA polymerase (RNAP) to a library of 96 random sequences in parallel. These results establish SPACE as a simple, easy to implement, and massively parallelizable platform for continuous directed evolution in general laboratories. John Wiley and Sons Inc. 2022-09-21 /pmc/articles/PMC9491160/ /pubmed/36129229 http://dx.doi.org/10.15252/msb.202210934 Text en © 2022 The Authors. Published under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Wei, Ting Lai, Wangsheng Chen, Qian Zhang, Yi Sun, Chenjian He, Xionglei Zhao, Guoping Fu, Xiongfei Liu, Chenli Exploiting spatial dimensions to enable parallelized continuous directed evolution |
title | Exploiting spatial dimensions to enable parallelized continuous directed evolution |
title_full | Exploiting spatial dimensions to enable parallelized continuous directed evolution |
title_fullStr | Exploiting spatial dimensions to enable parallelized continuous directed evolution |
title_full_unstemmed | Exploiting spatial dimensions to enable parallelized continuous directed evolution |
title_short | Exploiting spatial dimensions to enable parallelized continuous directed evolution |
title_sort | exploiting spatial dimensions to enable parallelized continuous directed evolution |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491160/ https://www.ncbi.nlm.nih.gov/pubmed/36129229 http://dx.doi.org/10.15252/msb.202210934 |
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