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Thermo-Programmed Synthetic DNA-Based Receptors
[Image: see text] Herein, we present a generalizable and versatile strategy to engineer synthetic DNA ligand-binding devices that can be programmed to load and release a specific ligand at a defined temperature. We do so by re-engineering two model DNA-based receptors: a triplex-forming bivalent DNA...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933611/ https://www.ncbi.nlm.nih.gov/pubmed/36689298 http://dx.doi.org/10.1021/acsnano.2c07039 |
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author | Mariottini, Davide Idili, Andrea Ercolani, Gianfranco Ricci, Francesco |
author_facet | Mariottini, Davide Idili, Andrea Ercolani, Gianfranco Ricci, Francesco |
author_sort | Mariottini, Davide |
collection | PubMed |
description | [Image: see text] Herein, we present a generalizable and versatile strategy to engineer synthetic DNA ligand-binding devices that can be programmed to load and release a specific ligand at a defined temperature. We do so by re-engineering two model DNA-based receptors: a triplex-forming bivalent DNA-based receptor that recognizes a specific DNA sequence and an ATP-binding aptamer. The temperature at which these receptors load/release their ligands can be finely modulated by controlling the entropy associated with the linker connecting the two ligand-binding domains. The availability of a set of receptors with tunable and reversible temperature dependence allows achieving complex load/release behavior such as sustained ligand release over a wide temperature range. Similar programmable thermo-responsive synthetic ligand-binding devices can be of utility in applications such as drug delivery and production of smart materials. |
format | Online Article Text |
id | pubmed-9933611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99336112023-02-17 Thermo-Programmed Synthetic DNA-Based Receptors Mariottini, Davide Idili, Andrea Ercolani, Gianfranco Ricci, Francesco ACS Nano [Image: see text] Herein, we present a generalizable and versatile strategy to engineer synthetic DNA ligand-binding devices that can be programmed to load and release a specific ligand at a defined temperature. We do so by re-engineering two model DNA-based receptors: a triplex-forming bivalent DNA-based receptor that recognizes a specific DNA sequence and an ATP-binding aptamer. The temperature at which these receptors load/release their ligands can be finely modulated by controlling the entropy associated with the linker connecting the two ligand-binding domains. The availability of a set of receptors with tunable and reversible temperature dependence allows achieving complex load/release behavior such as sustained ligand release over a wide temperature range. Similar programmable thermo-responsive synthetic ligand-binding devices can be of utility in applications such as drug delivery and production of smart materials. American Chemical Society 2023-01-23 /pmc/articles/PMC9933611/ /pubmed/36689298 http://dx.doi.org/10.1021/acsnano.2c07039 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Mariottini, Davide Idili, Andrea Ercolani, Gianfranco Ricci, Francesco Thermo-Programmed Synthetic DNA-Based Receptors |
title | Thermo-Programmed
Synthetic DNA-Based Receptors |
title_full | Thermo-Programmed
Synthetic DNA-Based Receptors |
title_fullStr | Thermo-Programmed
Synthetic DNA-Based Receptors |
title_full_unstemmed | Thermo-Programmed
Synthetic DNA-Based Receptors |
title_short | Thermo-Programmed
Synthetic DNA-Based Receptors |
title_sort | thermo-programmed
synthetic dna-based receptors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933611/ https://www.ncbi.nlm.nih.gov/pubmed/36689298 http://dx.doi.org/10.1021/acsnano.2c07039 |
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