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DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids

DNA nanotechnology provides a promising approach for the development of biomedical point-of-care diagnostic nanoscale devices that are easy to use and cost-effective, highly sensitive and thus constitute an alternative to expensive, complex diagnostic devices. Moreover, DNA nanotechnology-based devi...

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Autores principales: Domljanovic, Ivana, Loretan, Morgane, Kempter, Susanne, Acuna, Guillermo P., Kocabey, Samet, Ruegg, Curzio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612396/
https://www.ncbi.nlm.nih.gov/pubmed/36219167
http://dx.doi.org/10.1039/d2nr03985k
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author Domljanovic, Ivana
Loretan, Morgane
Kempter, Susanne
Acuna, Guillermo P.
Kocabey, Samet
Ruegg, Curzio
author_facet Domljanovic, Ivana
Loretan, Morgane
Kempter, Susanne
Acuna, Guillermo P.
Kocabey, Samet
Ruegg, Curzio
author_sort Domljanovic, Ivana
collection PubMed
description DNA nanotechnology provides a promising approach for the development of biomedical point-of-care diagnostic nanoscale devices that are easy to use and cost-effective, highly sensitive and thus constitute an alternative to expensive, complex diagnostic devices. Moreover, DNA nanotechnology-based devices are particularly advantageous for applications in oncology, owing to being ideally suited for the detection of cancer-associated nucleic acids, including circulating tumor-derived DNA fragments (ctDNAs), circulating microRNAs (miRNAs) and other RNA species. Here, we present a dynamic DNA origami book biosensor that is precisely decorated with arrays of fluorophores acting as donors and acceptors and also fluorescence quenchers that produce a strong optical readout upon exposure to external stimuli for the single or dual detection of target oligonucleotides and miRNAs. This biosensor allowed the detection of target molecules either through the decrease of Förster resonance energy transfer (FRET) or an increase in the fluorescence intensity profile owing to a rotation of the constituent top layer of the structure. Single-DNA origami experiments showed that detection of two targets can be achieved simultaneously within 10 min with a limit of detection in the range of 1–10 pM. Overall, our DNA origami book biosensor design showed sensitive and specific detection of synthetic target oligonucleotides and natural miRNAs extracted from cancer cells. Based on these results, we foresee that our DNA origami biosensor may be developed into a cost-effective point-of-care diagnostic strategy for the specific and sensitive detection of a variety of DNAs and RNAs, such as ctDNAs, miRNAs, mRNAs, and viral DNA/RNAs in human samples.
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spelling pubmed-96123962022-11-07 DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids Domljanovic, Ivana Loretan, Morgane Kempter, Susanne Acuna, Guillermo P. Kocabey, Samet Ruegg, Curzio Nanoscale Chemistry DNA nanotechnology provides a promising approach for the development of biomedical point-of-care diagnostic nanoscale devices that are easy to use and cost-effective, highly sensitive and thus constitute an alternative to expensive, complex diagnostic devices. Moreover, DNA nanotechnology-based devices are particularly advantageous for applications in oncology, owing to being ideally suited for the detection of cancer-associated nucleic acids, including circulating tumor-derived DNA fragments (ctDNAs), circulating microRNAs (miRNAs) and other RNA species. Here, we present a dynamic DNA origami book biosensor that is precisely decorated with arrays of fluorophores acting as donors and acceptors and also fluorescence quenchers that produce a strong optical readout upon exposure to external stimuli for the single or dual detection of target oligonucleotides and miRNAs. This biosensor allowed the detection of target molecules either through the decrease of Förster resonance energy transfer (FRET) or an increase in the fluorescence intensity profile owing to a rotation of the constituent top layer of the structure. Single-DNA origami experiments showed that detection of two targets can be achieved simultaneously within 10 min with a limit of detection in the range of 1–10 pM. Overall, our DNA origami book biosensor design showed sensitive and specific detection of synthetic target oligonucleotides and natural miRNAs extracted from cancer cells. Based on these results, we foresee that our DNA origami biosensor may be developed into a cost-effective point-of-care diagnostic strategy for the specific and sensitive detection of a variety of DNAs and RNAs, such as ctDNAs, miRNAs, mRNAs, and viral DNA/RNAs in human samples. The Royal Society of Chemistry 2022-10-11 /pmc/articles/PMC9612396/ /pubmed/36219167 http://dx.doi.org/10.1039/d2nr03985k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Domljanovic, Ivana
Loretan, Morgane
Kempter, Susanne
Acuna, Guillermo P.
Kocabey, Samet
Ruegg, Curzio
DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids
title DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids
title_full DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids
title_fullStr DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids
title_full_unstemmed DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids
title_short DNA origami book biosensor for multiplex detection of cancer-associated nucleic acids
title_sort dna origami book biosensor for multiplex detection of cancer-associated nucleic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612396/
https://www.ncbi.nlm.nih.gov/pubmed/36219167
http://dx.doi.org/10.1039/d2nr03985k
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