Cargando…
Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides
BACKGROUND: Short nucleic acid oligomers have found a wide range of applications in experimental physics, biology and medicine, and show potential for the treatment of acquired and genetic diseases. These applications rely heavily on the predictability of hybridization through Watson–Crick base pair...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887185/ https://www.ncbi.nlm.nih.gov/pubmed/29622040 http://dx.doi.org/10.1186/s12951-018-0361-2 |
_version_ | 1783312243314655232 |
---|---|
author | de Bruin, Donny Bossert, Nelli Aartsma-Rus, Annemieke Bouwmeester, Dirk |
author_facet | de Bruin, Donny Bossert, Nelli Aartsma-Rus, Annemieke Bouwmeester, Dirk |
author_sort | de Bruin, Donny |
collection | PubMed |
description | BACKGROUND: Short nucleic acid oligomers have found a wide range of applications in experimental physics, biology and medicine, and show potential for the treatment of acquired and genetic diseases. These applications rely heavily on the predictability of hybridization through Watson–Crick base pairing to allow positioning on a nanometer scale, as well as binding to the target transcripts, but also off-target binding to transcripts with partial homology. These effects are of particular importance in the development of therapeutic oligonucleotides, where off-target effects caused by the binding of mismatched sequences need to be avoided. RESULTS: We employ a novel method of probing DNA hybridization using optically active DNA-stabilized silver clusters (Ag-DNA) to measure binding efficiencies through a change in fluorescence intensity. In this way we can determine their location-specific sensitivity to individual mismatches in the sequence. The results reveal a strong dependence of the hybridization on the location of the mismatch, whereby mismatches close to the edges and center show a relatively minor impact. In parallel, we propose a simple model for calculating the annealing ratios of mismatched DNA sequences, which supports our experimental results. CONCLUSION: The primary result shown in this work is a demonstration of a novel technique to measure DNA hybridization using fluorescent Ag-DNA. With this technique, we investigated the effect of mismatches on the hybridization efficiency, and found a significant dependence on the location of individual mismatches. These effects are strongly influenced by the length of the used oligonucleotides. The novel probe method based on fluorescent Ag-DNA functions as a reliable tool in measuring this behavior. As a secondary result, we formulated a simple model that is consistent with the experimental data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0361-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5887185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58871852018-04-09 Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides de Bruin, Donny Bossert, Nelli Aartsma-Rus, Annemieke Bouwmeester, Dirk J Nanobiotechnology Research BACKGROUND: Short nucleic acid oligomers have found a wide range of applications in experimental physics, biology and medicine, and show potential for the treatment of acquired and genetic diseases. These applications rely heavily on the predictability of hybridization through Watson–Crick base pairing to allow positioning on a nanometer scale, as well as binding to the target transcripts, but also off-target binding to transcripts with partial homology. These effects are of particular importance in the development of therapeutic oligonucleotides, where off-target effects caused by the binding of mismatched sequences need to be avoided. RESULTS: We employ a novel method of probing DNA hybridization using optically active DNA-stabilized silver clusters (Ag-DNA) to measure binding efficiencies through a change in fluorescence intensity. In this way we can determine their location-specific sensitivity to individual mismatches in the sequence. The results reveal a strong dependence of the hybridization on the location of the mismatch, whereby mismatches close to the edges and center show a relatively minor impact. In parallel, we propose a simple model for calculating the annealing ratios of mismatched DNA sequences, which supports our experimental results. CONCLUSION: The primary result shown in this work is a demonstration of a novel technique to measure DNA hybridization using fluorescent Ag-DNA. With this technique, we investigated the effect of mismatches on the hybridization efficiency, and found a significant dependence on the location of individual mismatches. These effects are strongly influenced by the length of the used oligonucleotides. The novel probe method based on fluorescent Ag-DNA functions as a reliable tool in measuring this behavior. As a secondary result, we formulated a simple model that is consistent with the experimental data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0361-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-06 /pmc/articles/PMC5887185/ /pubmed/29622040 http://dx.doi.org/10.1186/s12951-018-0361-2 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research de Bruin, Donny Bossert, Nelli Aartsma-Rus, Annemieke Bouwmeester, Dirk Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
title | Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
title_full | Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
title_fullStr | Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
title_full_unstemmed | Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
title_short | Measuring DNA hybridization using fluorescent DNA-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
title_sort | measuring dna hybridization using fluorescent dna-stabilized silver clusters to investigate mismatch effects on therapeutic oligonucleotides |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887185/ https://www.ncbi.nlm.nih.gov/pubmed/29622040 http://dx.doi.org/10.1186/s12951-018-0361-2 |
work_keys_str_mv | AT debruindonny measuringdnahybridizationusingfluorescentdnastabilizedsilverclusterstoinvestigatemismatcheffectsontherapeuticoligonucleotides AT bossertnelli measuringdnahybridizationusingfluorescentdnastabilizedsilverclusterstoinvestigatemismatcheffectsontherapeuticoligonucleotides AT aartsmarusannemieke measuringdnahybridizationusingfluorescentdnastabilizedsilverclusterstoinvestigatemismatcheffectsontherapeuticoligonucleotides AT bouwmeesterdirk measuringdnahybridizationusingfluorescentdnastabilizedsilverclusterstoinvestigatemismatcheffectsontherapeuticoligonucleotides |