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Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles

A modified non-cross-linking gold-nanoparticles (Au-NPs) aggregation strategy has been developed for the label free colorimetric detection of DNAs/RNAs based on self-assembling target species in the presence of thiolated probes. Two complementary thiol- modified probes, each of which specifically bi...

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Autores principales: Shokri, Ehsan, Hosseini, Morteza, Davari, Mehdi D., Ganjali, Mohammad R., Peppelenbosch, Maikel P., Rezaee, Farhad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384278/
https://www.ncbi.nlm.nih.gov/pubmed/28387331
http://dx.doi.org/10.1038/srep45837
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author Shokri, Ehsan
Hosseini, Morteza
Davari, Mehdi D.
Ganjali, Mohammad R.
Peppelenbosch, Maikel P.
Rezaee, Farhad
author_facet Shokri, Ehsan
Hosseini, Morteza
Davari, Mehdi D.
Ganjali, Mohammad R.
Peppelenbosch, Maikel P.
Rezaee, Farhad
author_sort Shokri, Ehsan
collection PubMed
description A modified non-cross-linking gold-nanoparticles (Au-NPs) aggregation strategy has been developed for the label free colorimetric detection of DNAs/RNAs based on self-assembling target species in the presence of thiolated probes. Two complementary thiol- modified probes, each of which specifically binds at one half of the target introduced SH groups at both ends of dsDNA. Continuous disulfide bond formation at 3′ and 5′ terminals of targets leads to the self-assembly of dsDNAs into the sulfur- rich and flexible products with different lengths. These products have a high affinity for the surface of Au-NPs and efficiently protect the surface from salt induced aggregation. To evaluate the assay efficacy, a small part of the citrus tristeza virus (CTV) genome was targeted, leading to a detection limit of about 5 × 10(−9) mol.L(−1) over a linear ranged from 20 × 10(−9) to 10 × 10(−7) mol.L(−1). This approach also exhibits good reproducibility and recovery levels in the presence of plant total RNA or human plasma total circulating RNA extracts. Self-assembled targets can be then sensitively distinguished from non-assembled or mismatched targets after gel electrophoresis. The disulfide reaction method and integrating self-assembled DNAs/RNAs targets with bare AuNPs as a sensitive indicator provide us a powerful and simple visual detection tool for a wide range of applications.
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spelling pubmed-53842782017-04-11 Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles Shokri, Ehsan Hosseini, Morteza Davari, Mehdi D. Ganjali, Mohammad R. Peppelenbosch, Maikel P. Rezaee, Farhad Sci Rep Article A modified non-cross-linking gold-nanoparticles (Au-NPs) aggregation strategy has been developed for the label free colorimetric detection of DNAs/RNAs based on self-assembling target species in the presence of thiolated probes. Two complementary thiol- modified probes, each of which specifically binds at one half of the target introduced SH groups at both ends of dsDNA. Continuous disulfide bond formation at 3′ and 5′ terminals of targets leads to the self-assembly of dsDNAs into the sulfur- rich and flexible products with different lengths. These products have a high affinity for the surface of Au-NPs and efficiently protect the surface from salt induced aggregation. To evaluate the assay efficacy, a small part of the citrus tristeza virus (CTV) genome was targeted, leading to a detection limit of about 5 × 10(−9) mol.L(−1) over a linear ranged from 20 × 10(−9) to 10 × 10(−7) mol.L(−1). This approach also exhibits good reproducibility and recovery levels in the presence of plant total RNA or human plasma total circulating RNA extracts. Self-assembled targets can be then sensitively distinguished from non-assembled or mismatched targets after gel electrophoresis. The disulfide reaction method and integrating self-assembled DNAs/RNAs targets with bare AuNPs as a sensitive indicator provide us a powerful and simple visual detection tool for a wide range of applications. Nature Publishing Group 2017-04-07 /pmc/articles/PMC5384278/ /pubmed/28387331 http://dx.doi.org/10.1038/srep45837 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Shokri, Ehsan
Hosseini, Morteza
Davari, Mehdi D.
Ganjali, Mohammad R.
Peppelenbosch, Maikel P.
Rezaee, Farhad
Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles
title Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles
title_full Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles
title_fullStr Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles
title_full_unstemmed Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles
title_short Disulfide-induced self-assembled targets: A novel strategy for the label free colorimetric detection of DNAs/RNAs via unmodified gold nanoparticles
title_sort disulfide-induced self-assembled targets: a novel strategy for the label free colorimetric detection of dnas/rnas via unmodified gold nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384278/
https://www.ncbi.nlm.nih.gov/pubmed/28387331
http://dx.doi.org/10.1038/srep45837
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