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Surface Hybridization Chain Reaction of Binary Mixture DNA-PEG Corona Nanostructures Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly
[Image: see text] DNA-polymer hybrids have been attracting interest as adaptable functional materials by combining the stability of polymers with DNA nanotechnology. Both research fields have in common the capacity to be precise, versatile, and tunable, a prerequisite for creating powerful tools whi...
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/PMC10655036/ https://www.ncbi.nlm.nih.gov/pubmed/37844270 http://dx.doi.org/10.1021/acs.bioconjchem.3c00293 |
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author | Chaimueangchuen, Siriporn Frommer, Jennifer Ferguson, Calum T. J. O’Reilly, Rachel K. |
author_facet | Chaimueangchuen, Siriporn Frommer, Jennifer Ferguson, Calum T. J. O’Reilly, Rachel K. |
author_sort | Chaimueangchuen, Siriporn |
collection | PubMed |
description | [Image: see text] DNA-polymer hybrids have been attracting interest as adaptable functional materials by combining the stability of polymers with DNA nanotechnology. Both research fields have in common the capacity to be precise, versatile, and tunable, a prerequisite for creating powerful tools which can be easily tailored and adapted for bio-related applications. However, the conjugation of hydrophilic DNA with hydrophobic polymers remains challenging. In recent years, polymerization-induced self-assembly (PISA) has attracted significant attention for constructing nano-objects of various morphologies owing to the one-step nature of the process, creating a beneficial method for the creation of amphiphilic DNA-polymer nanostructures. This process not only allows pure DNA-polymer-based systems to be produced but also enables the mixture of other polymeric species with DNA conjugates. Here, we present the first report of a DNA-PEG corona nano-object’s synthesis without the addition of an external photoinitiator or photocatalyst via photo-PISA. Furthermore, this work shows the use of DNA-macroCTA, which was first synthesized using a solid-support method resulting in high yields, easy upscaling, and no need for HPLC purification. In addition, to the formation of DNA-polymer structures, increasing the nucleic acid loading of assemblies is of great importance. One of the most intriguing phenomena of DNA is the hybridization of single-stranded DNA with a second strand, increasing the nucleic acid content. However, hybridization of DNA in a particle corona may destabilize the nanomaterial due to the electrostatic repulsive force on the DNA corona. Here, we have investigated how changing the DNA volume fraction in hybrid DNA-polymer self-assembled material affects the morphology. Moreover, the effect of the corona composition on the stability of the system during the hybridization was studied. Additionally, the hybridization chain reaction was successfully applied as a new method to increase the amount of DNA on a DNA-based nano-object without disturbing the morphology achieving a fluorescence signal amplification. |
format | Online Article Text |
id | pubmed-10655036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106550362023-11-17 Surface Hybridization Chain Reaction of Binary Mixture DNA-PEG Corona Nanostructures Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly Chaimueangchuen, Siriporn Frommer, Jennifer Ferguson, Calum T. J. O’Reilly, Rachel K. Bioconjug Chem [Image: see text] DNA-polymer hybrids have been attracting interest as adaptable functional materials by combining the stability of polymers with DNA nanotechnology. Both research fields have in common the capacity to be precise, versatile, and tunable, a prerequisite for creating powerful tools which can be easily tailored and adapted for bio-related applications. However, the conjugation of hydrophilic DNA with hydrophobic polymers remains challenging. In recent years, polymerization-induced self-assembly (PISA) has attracted significant attention for constructing nano-objects of various morphologies owing to the one-step nature of the process, creating a beneficial method for the creation of amphiphilic DNA-polymer nanostructures. This process not only allows pure DNA-polymer-based systems to be produced but also enables the mixture of other polymeric species with DNA conjugates. Here, we present the first report of a DNA-PEG corona nano-object’s synthesis without the addition of an external photoinitiator or photocatalyst via photo-PISA. Furthermore, this work shows the use of DNA-macroCTA, which was first synthesized using a solid-support method resulting in high yields, easy upscaling, and no need for HPLC purification. In addition, to the formation of DNA-polymer structures, increasing the nucleic acid loading of assemblies is of great importance. One of the most intriguing phenomena of DNA is the hybridization of single-stranded DNA with a second strand, increasing the nucleic acid content. However, hybridization of DNA in a particle corona may destabilize the nanomaterial due to the electrostatic repulsive force on the DNA corona. Here, we have investigated how changing the DNA volume fraction in hybrid DNA-polymer self-assembled material affects the morphology. Moreover, the effect of the corona composition on the stability of the system during the hybridization was studied. Additionally, the hybridization chain reaction was successfully applied as a new method to increase the amount of DNA on a DNA-based nano-object without disturbing the morphology achieving a fluorescence signal amplification. American Chemical Society 2023-10-16 /pmc/articles/PMC10655036/ /pubmed/37844270 http://dx.doi.org/10.1021/acs.bioconjchem.3c00293 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 | Chaimueangchuen, Siriporn Frommer, Jennifer Ferguson, Calum T. J. O’Reilly, Rachel K. Surface Hybridization Chain Reaction of Binary Mixture DNA-PEG Corona Nanostructures Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly |
title | Surface
Hybridization Chain Reaction
of Binary Mixture DNA-PEG Corona Nanostructures
Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly |
title_full | Surface
Hybridization Chain Reaction
of Binary Mixture DNA-PEG Corona Nanostructures
Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly |
title_fullStr | Surface
Hybridization Chain Reaction
of Binary Mixture DNA-PEG Corona Nanostructures
Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly |
title_full_unstemmed | Surface
Hybridization Chain Reaction
of Binary Mixture DNA-PEG Corona Nanostructures
Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly |
title_short | Surface
Hybridization Chain Reaction
of Binary Mixture DNA-PEG Corona Nanostructures
Produced by Low-Volume RAFT-Mediated Photopolymerization-Induced Self-Assembly |
title_sort | surface
hybridization chain reaction
of binary mixture dna-peg corona nanostructures
produced by low-volume raft-mediated photopolymerization-induced self-assembly |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655036/ https://www.ncbi.nlm.nih.gov/pubmed/37844270 http://dx.doi.org/10.1021/acs.bioconjchem.3c00293 |
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