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Controllable DNA strand displacement by independent metal–ligand complexation
Introduction of artificial metal–ligand base pairs can enrich the structural diversity and functional controllability of nucleic acids. In this work, we revealed a novel approach by placing a ligand-type nucleoside as an independent toehold to control DNA strand-displacement reactions based on metal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246113/ https://www.ncbi.nlm.nih.gov/pubmed/34257868 http://dx.doi.org/10.1039/d1sc01041g |
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author | Wang, Liang-Liang Zhang, Qiu-Long Wang, Yang Liu, Yan Lin, Jiao Xie, Fan Xu, Liang |
author_facet | Wang, Liang-Liang Zhang, Qiu-Long Wang, Yang Liu, Yan Lin, Jiao Xie, Fan Xu, Liang |
author_sort | Wang, Liang-Liang |
collection | PubMed |
description | Introduction of artificial metal–ligand base pairs can enrich the structural diversity and functional controllability of nucleic acids. In this work, we revealed a novel approach by placing a ligand-type nucleoside as an independent toehold to control DNA strand-displacement reactions based on metal–ligand complexation. This metal-mediated artificial base pair could initiate strand invasion similar to the natural toehold DNA, but exhibited flexible controllability to manipulate the dynamics of strand displacement that was only governed by its intrinsic coordination properties. External factors that influence the intrinsic properties of metal–ligand complexation, including metal species, metal concentrations and pH conditions, could be utilized to regulate the strand dynamics. Reversible control of DNA strand-displacement reactions was also achieved through combination of the metal-mediated artificial base pair with the conventional toehold-mediated strand exchange by cyclical treatments of the metal ion and the chelating reagent. Unlike previous studies of embedded metal-mediated base pairs within natural base pairs, this metal–ligand complexation is not integrated into the nucleic acid structure, but functions as an independent toehold to regulate strand displacement, which would open a new door for the development of versatile dynamic DNA nanotechnologies. |
format | Online Article Text |
id | pubmed-8246113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-82461132021-07-12 Controllable DNA strand displacement by independent metal–ligand complexation Wang, Liang-Liang Zhang, Qiu-Long Wang, Yang Liu, Yan Lin, Jiao Xie, Fan Xu, Liang Chem Sci Chemistry Introduction of artificial metal–ligand base pairs can enrich the structural diversity and functional controllability of nucleic acids. In this work, we revealed a novel approach by placing a ligand-type nucleoside as an independent toehold to control DNA strand-displacement reactions based on metal–ligand complexation. This metal-mediated artificial base pair could initiate strand invasion similar to the natural toehold DNA, but exhibited flexible controllability to manipulate the dynamics of strand displacement that was only governed by its intrinsic coordination properties. External factors that influence the intrinsic properties of metal–ligand complexation, including metal species, metal concentrations and pH conditions, could be utilized to regulate the strand dynamics. Reversible control of DNA strand-displacement reactions was also achieved through combination of the metal-mediated artificial base pair with the conventional toehold-mediated strand exchange by cyclical treatments of the metal ion and the chelating reagent. Unlike previous studies of embedded metal-mediated base pairs within natural base pairs, this metal–ligand complexation is not integrated into the nucleic acid structure, but functions as an independent toehold to regulate strand displacement, which would open a new door for the development of versatile dynamic DNA nanotechnologies. The Royal Society of Chemistry 2021-05-18 /pmc/articles/PMC8246113/ /pubmed/34257868 http://dx.doi.org/10.1039/d1sc01041g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wang, Liang-Liang Zhang, Qiu-Long Wang, Yang Liu, Yan Lin, Jiao Xie, Fan Xu, Liang Controllable DNA strand displacement by independent metal–ligand complexation |
title | Controllable DNA strand displacement by independent metal–ligand complexation |
title_full | Controllable DNA strand displacement by independent metal–ligand complexation |
title_fullStr | Controllable DNA strand displacement by independent metal–ligand complexation |
title_full_unstemmed | Controllable DNA strand displacement by independent metal–ligand complexation |
title_short | Controllable DNA strand displacement by independent metal–ligand complexation |
title_sort | controllable dna strand displacement by independent metal–ligand complexation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246113/ https://www.ncbi.nlm.nih.gov/pubmed/34257868 http://dx.doi.org/10.1039/d1sc01041g |
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