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A redox-based electrogenetic CRISPR system to connect with and control biological information networks
Electronic information can be transmitted to cells directly from microelectronics via electrode-activated redox mediators. These transmissions are decoded by redox-responsive promoters which enable user-specified control over biological function. Here, we build on this redox communication modality b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7228920/ https://www.ncbi.nlm.nih.gov/pubmed/32415193 http://dx.doi.org/10.1038/s41467-020-16249-x |
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author | Bhokisham, Narendranath VanArsdale, Eric Stephens, Kristina T. Hauk, Pricila Payne, Gregory F. Bentley, William E. |
author_facet | Bhokisham, Narendranath VanArsdale, Eric Stephens, Kristina T. Hauk, Pricila Payne, Gregory F. Bentley, William E. |
author_sort | Bhokisham, Narendranath |
collection | PubMed |
description | Electronic information can be transmitted to cells directly from microelectronics via electrode-activated redox mediators. These transmissions are decoded by redox-responsive promoters which enable user-specified control over biological function. Here, we build on this redox communication modality by establishing an electronic eCRISPR conduit of information exchange. This system acts as a biological signal processor, amplifying signal reception and filtering biological noise. We electronically amplify bacterial quorum sensing (QS) signaling by activating LasI, the autoinducer-1 synthase. Similarly, we filter out unintended noise by inhibiting the native SoxRS-mediated oxidative stress response regulon. We then construct an eCRISPR based redox conduit in both E. coli and Salmonella enterica. Finally, we display eCRISPR based information processing that allows transmission of spatiotemporal redox commands which are then decoded by gelatin-encapsulated E. coli. We anticipate that redox communication channels will enable biohybrid microelectronic devices that could transform our abilities to electronically interpret and control biological function. |
format | Online Article Text |
id | pubmed-7228920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72289202020-06-05 A redox-based electrogenetic CRISPR system to connect with and control biological information networks Bhokisham, Narendranath VanArsdale, Eric Stephens, Kristina T. Hauk, Pricila Payne, Gregory F. Bentley, William E. Nat Commun Article Electronic information can be transmitted to cells directly from microelectronics via electrode-activated redox mediators. These transmissions are decoded by redox-responsive promoters which enable user-specified control over biological function. Here, we build on this redox communication modality by establishing an electronic eCRISPR conduit of information exchange. This system acts as a biological signal processor, amplifying signal reception and filtering biological noise. We electronically amplify bacterial quorum sensing (QS) signaling by activating LasI, the autoinducer-1 synthase. Similarly, we filter out unintended noise by inhibiting the native SoxRS-mediated oxidative stress response regulon. We then construct an eCRISPR based redox conduit in both E. coli and Salmonella enterica. Finally, we display eCRISPR based information processing that allows transmission of spatiotemporal redox commands which are then decoded by gelatin-encapsulated E. coli. We anticipate that redox communication channels will enable biohybrid microelectronic devices that could transform our abilities to electronically interpret and control biological function. Nature Publishing Group UK 2020-05-15 /pmc/articles/PMC7228920/ /pubmed/32415193 http://dx.doi.org/10.1038/s41467-020-16249-x 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 Bhokisham, Narendranath VanArsdale, Eric Stephens, Kristina T. Hauk, Pricila Payne, Gregory F. Bentley, William E. A redox-based electrogenetic CRISPR system to connect with and control biological information networks |
title | A redox-based electrogenetic CRISPR system to connect with and control biological information networks |
title_full | A redox-based electrogenetic CRISPR system to connect with and control biological information networks |
title_fullStr | A redox-based electrogenetic CRISPR system to connect with and control biological information networks |
title_full_unstemmed | A redox-based electrogenetic CRISPR system to connect with and control biological information networks |
title_short | A redox-based electrogenetic CRISPR system to connect with and control biological information networks |
title_sort | redox-based electrogenetic crispr system to connect with and control biological information networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7228920/ https://www.ncbi.nlm.nih.gov/pubmed/32415193 http://dx.doi.org/10.1038/s41467-020-16249-x |
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