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Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics
In recent years, DNA computing frameworks have been developed to create dynamical systems which can be used for information processing. These emerging synthetic biochemistry tools can be leveraged to gain a better understanding of fundamental biology but can also be implemented in biosensors and unc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913268/ https://www.ncbi.nlm.nih.gov/pubmed/29686392 http://dx.doi.org/10.1038/s41598-018-24659-7 |
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author | Kurylo, Ievgen Gines, Guillaume Rondelez, Yannick Coffinier, Yannick Vlandas, Alexis |
author_facet | Kurylo, Ievgen Gines, Guillaume Rondelez, Yannick Coffinier, Yannick Vlandas, Alexis |
author_sort | Kurylo, Ievgen |
collection | PubMed |
description | In recent years, DNA computing frameworks have been developed to create dynamical systems which can be used for information processing. These emerging synthetic biochemistry tools can be leveraged to gain a better understanding of fundamental biology but can also be implemented in biosensors and unconventional computing. Most of the efforts so far have focused on changing the topologies of DNA molecular networks or scaling them up. Several issues have thus received little attention and remain to be solved to turn them into real life technologies. In particular, the ability to easily interact in real-time with them is a key requirement. The previous attempts to achieve this aim have used microfluidic approaches, such as valves, which are cumbersome. We show that electrochemical triggering using DNA-grafted micro-fabricated gold electrodes can be used to give instructions to these molecular systems. We demonstrate how this approach can be used to release at specific times and locations DNA- based instructions. In particular, we trigger reaction-diffusion autocatalytic fronts in microfluidic channels. While limited by the stability of the Au-S bond, this easy to implement, versatile and scalable technique can be used in any biology laboratory to provide new ways to interact with any DNA-based computing framework. |
format | Online Article Text |
id | pubmed-5913268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59132682018-04-30 Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics Kurylo, Ievgen Gines, Guillaume Rondelez, Yannick Coffinier, Yannick Vlandas, Alexis Sci Rep Article In recent years, DNA computing frameworks have been developed to create dynamical systems which can be used for information processing. These emerging synthetic biochemistry tools can be leveraged to gain a better understanding of fundamental biology but can also be implemented in biosensors and unconventional computing. Most of the efforts so far have focused on changing the topologies of DNA molecular networks or scaling them up. Several issues have thus received little attention and remain to be solved to turn them into real life technologies. In particular, the ability to easily interact in real-time with them is a key requirement. The previous attempts to achieve this aim have used microfluidic approaches, such as valves, which are cumbersome. We show that electrochemical triggering using DNA-grafted micro-fabricated gold electrodes can be used to give instructions to these molecular systems. We demonstrate how this approach can be used to release at specific times and locations DNA- based instructions. In particular, we trigger reaction-diffusion autocatalytic fronts in microfluidic channels. While limited by the stability of the Au-S bond, this easy to implement, versatile and scalable technique can be used in any biology laboratory to provide new ways to interact with any DNA-based computing framework. Nature Publishing Group UK 2018-04-23 /pmc/articles/PMC5913268/ /pubmed/29686392 http://dx.doi.org/10.1038/s41598-018-24659-7 Text en © The Author(s) 2018 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 Kurylo, Ievgen Gines, Guillaume Rondelez, Yannick Coffinier, Yannick Vlandas, Alexis Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics |
title | Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics |
title_full | Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics |
title_fullStr | Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics |
title_full_unstemmed | Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics |
title_short | Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics |
title_sort | spatiotemporal control of dna-based chemical reaction network via electrochemical activation in microfluidics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913268/ https://www.ncbi.nlm.nih.gov/pubmed/29686392 http://dx.doi.org/10.1038/s41598-018-24659-7 |
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