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Nucleic acid strand displacement – from DNA nanotechnology to translational regulation
Nucleic acid strand displacement reactions involve the competition of two or more DNA or RNA strands of similar sequence for binding to a complementary strand, and facilitate the isothermal replacement of an incumbent strand by an invader. The process can be biased by augmenting the duplex comprisin...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132225/ https://www.ncbi.nlm.nih.gov/pubmed/37095744 http://dx.doi.org/10.1080/15476286.2023.2204565 |
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author | Simmel, Friedrich C. |
author_facet | Simmel, Friedrich C. |
author_sort | Simmel, Friedrich C. |
collection | PubMed |
description | Nucleic acid strand displacement reactions involve the competition of two or more DNA or RNA strands of similar sequence for binding to a complementary strand, and facilitate the isothermal replacement of an incumbent strand by an invader. The process can be biased by augmenting the duplex comprising the incumbent with a single-stranded extension, which can act as a toehold for a complementary invader. The toehold gives the invader a thermodynamic advantage over the incumbent, and can be programmed as a unique label to activate a specific strand displacement process. Toehold-mediated strand displacement processes have been extensively utilized for the operation of DNA-based molecular machines and devices as well as for the design of DNA-based chemical reaction networks. More recently, principles developed initially in the context of DNA nanotechnology have been applied for the de novo design of gene regulatory switches that can operate inside living cells. The article specifically focuses on the design of RNA-based translational regulators termed toehold switches. Toehold switches utilize toehold-mediated strand invasion to either activate or repress translation of an mRNA in response to the binding of a trigger RNA molecule. The basic operation principles of toehold switches will be discussed as well as their applications in sensing and biocomputing. Finally, strategies for their optimization will be described as well as challenges for their operation in vivo. |
format | Online Article Text |
id | pubmed-10132225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-101322252023-04-27 Nucleic acid strand displacement – from DNA nanotechnology to translational regulation Simmel, Friedrich C. RNA Biol Review Nucleic acid strand displacement reactions involve the competition of two or more DNA or RNA strands of similar sequence for binding to a complementary strand, and facilitate the isothermal replacement of an incumbent strand by an invader. The process can be biased by augmenting the duplex comprising the incumbent with a single-stranded extension, which can act as a toehold for a complementary invader. The toehold gives the invader a thermodynamic advantage over the incumbent, and can be programmed as a unique label to activate a specific strand displacement process. Toehold-mediated strand displacement processes have been extensively utilized for the operation of DNA-based molecular machines and devices as well as for the design of DNA-based chemical reaction networks. More recently, principles developed initially in the context of DNA nanotechnology have been applied for the de novo design of gene regulatory switches that can operate inside living cells. The article specifically focuses on the design of RNA-based translational regulators termed toehold switches. Toehold switches utilize toehold-mediated strand invasion to either activate or repress translation of an mRNA in response to the binding of a trigger RNA molecule. The basic operation principles of toehold switches will be discussed as well as their applications in sensing and biocomputing. Finally, strategies for their optimization will be described as well as challenges for their operation in vivo. Taylor & Francis 2023-04-24 /pmc/articles/PMC10132225/ /pubmed/37095744 http://dx.doi.org/10.1080/15476286.2023.2204565 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Review Simmel, Friedrich C. Nucleic acid strand displacement – from DNA nanotechnology to translational regulation |
title | Nucleic acid strand displacement – from DNA nanotechnology to translational regulation |
title_full | Nucleic acid strand displacement – from DNA nanotechnology to translational regulation |
title_fullStr | Nucleic acid strand displacement – from DNA nanotechnology to translational regulation |
title_full_unstemmed | Nucleic acid strand displacement – from DNA nanotechnology to translational regulation |
title_short | Nucleic acid strand displacement – from DNA nanotechnology to translational regulation |
title_sort | nucleic acid strand displacement – from dna nanotechnology to translational regulation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132225/ https://www.ncbi.nlm.nih.gov/pubmed/37095744 http://dx.doi.org/10.1080/15476286.2023.2204565 |
work_keys_str_mv | AT simmelfriedrichc nucleicacidstranddisplacementfromdnananotechnologytotranslationalregulation |