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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...

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Autores principales: Wei, Ting, Lai, Wangsheng, Chen, Qian, Zhang, Yi, Sun, Chenjian, He, Xionglei, Zhao, Guoping, Fu, Xiongfei, Liu, Chenli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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