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Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA
In this paper we describe a molecular beacon format assay in which encoded nanowire particles are used to achieve multiplexing. We demonstrate this principle with the detection of five viral pathogens; Hepatitis A virus, Hepatitis C virus, West Nile Virus, Human Immune Deficiency virus and Severe Ac...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Humana Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091129/ https://www.ncbi.nlm.nih.gov/pubmed/32218710 http://dx.doi.org/10.1385/NBT:1:4:327 |
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author | Sha, Michael Y. Yamanaka, Mark Walton, Ian D. Norton, Scott M. Stoermer, Rebecca L. Keating, Christine D. Natan, Michael J. Penn, Sharron G. |
author_facet | Sha, Michael Y. Yamanaka, Mark Walton, Ian D. Norton, Scott M. Stoermer, Rebecca L. Keating, Christine D. Natan, Michael J. Penn, Sharron G. |
author_sort | Sha, Michael Y. |
collection | PubMed |
description | In this paper we describe a molecular beacon format assay in which encoded nanowire particles are used to achieve multiplexing. We demonstrate this principle with the detection of five viral pathogens; Hepatitis A virus, Hepatitis C virus, West Nile Virus, Human Immune Deficiency virus and Severe Acute Respiratory Syndrome virus. Oligonucleotides are designed complementary to a target sequence of interest containing a 3′ universal fluorescence dye. A 5′ thiol causes the oligonucleotides to self-assemble onto the metal nanowire. The single-stranded oligonucleotide contains a self-complementary hairpin stem sequence of 10 bases that forces the 3′ fluorophore to come into contact with the metallic nanowire surface, thereby quenching the fluorescence. Upon addition of target DNA, there is hybridization with the complementary oligonucleotides. The resulting DNA hybrid is rigid, unfolds the hairpin structure, and causes the fluorophore to be moved away from the surface such that it is no longer quenched. By using differently encoded nanowires, each conjugated with a different oligonucleotide sequence, multiplexed DNA assays are possible using a single fluorophore, from a multiplexed RT-PCR reaction. |
format | Online Article Text |
id | pubmed-7091129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Humana Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70911292020-03-24 Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA Sha, Michael Y. Yamanaka, Mark Walton, Ian D. Norton, Scott M. Stoermer, Rebecca L. Keating, Christine D. Natan, Michael J. Penn, Sharron G. Nanobiotechnology Original Article In this paper we describe a molecular beacon format assay in which encoded nanowire particles are used to achieve multiplexing. We demonstrate this principle with the detection of five viral pathogens; Hepatitis A virus, Hepatitis C virus, West Nile Virus, Human Immune Deficiency virus and Severe Acute Respiratory Syndrome virus. Oligonucleotides are designed complementary to a target sequence of interest containing a 3′ universal fluorescence dye. A 5′ thiol causes the oligonucleotides to self-assemble onto the metal nanowire. The single-stranded oligonucleotide contains a self-complementary hairpin stem sequence of 10 bases that forces the 3′ fluorophore to come into contact with the metallic nanowire surface, thereby quenching the fluorescence. Upon addition of target DNA, there is hybridization with the complementary oligonucleotides. The resulting DNA hybrid is rigid, unfolds the hairpin structure, and causes the fluorophore to be moved away from the surface such that it is no longer quenched. By using differently encoded nanowires, each conjugated with a different oligonucleotide sequence, multiplexed DNA assays are possible using a single fluorophore, from a multiplexed RT-PCR reaction. Humana Press 2005 /pmc/articles/PMC7091129/ /pubmed/32218710 http://dx.doi.org/10.1385/NBT:1:4:327 Text en © Humana Press Inc 2005 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Sha, Michael Y. Yamanaka, Mark Walton, Ian D. Norton, Scott M. Stoermer, Rebecca L. Keating, Christine D. Natan, Michael J. Penn, Sharron G. Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA |
title | Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA |
title_full | Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA |
title_fullStr | Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA |
title_full_unstemmed | Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA |
title_short | Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA |
title_sort | encoded metal nanoparticle-based molecular beacons for multiplexed detection of dna |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091129/ https://www.ncbi.nlm.nih.gov/pubmed/32218710 http://dx.doi.org/10.1385/NBT:1:4:327 |
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