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Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif
DNA origami is an emerging technology that assembles hundreds of staple strands and one single-strand DNA into certain nanopattern. It has been widely used in various fields including detection of biological molecules such as DNA, RNA and proteins. MicroRNAs (miRNAs) play important roles in post-tra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749204/ https://www.ncbi.nlm.nih.gov/pubmed/23990889 http://dx.doi.org/10.1371/journal.pone.0069856 |
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author | Zhu, Jie Feng, Xiaolu Lou, Jingyu Li, Weidong Li, Sheng Zhu, Hongxin Yang, Lun Zhang, Aiping He, Lin Li, Can |
author_facet | Zhu, Jie Feng, Xiaolu Lou, Jingyu Li, Weidong Li, Sheng Zhu, Hongxin Yang, Lun Zhang, Aiping He, Lin Li, Can |
author_sort | Zhu, Jie |
collection | PubMed |
description | DNA origami is an emerging technology that assembles hundreds of staple strands and one single-strand DNA into certain nanopattern. It has been widely used in various fields including detection of biological molecules such as DNA, RNA and proteins. MicroRNAs (miRNAs) play important roles in post-transcriptional gene repression as well as many other biological processes such as cell growth and differentiation. Alterations of miRNAs' expression contribute to many human diseases. However, it is still a challenge to quantitatively detect miRNAs by origami technology. In this study, we developed a novel approach based on streptavidin and quantum dots binding complex (STV-QDs) labeled single strand displacement reaction on DNA origami to quantitatively detect the concentration of miRNAs. We illustrated a linear relationship between the concentration of an exemplary miRNA as miRNA-133 and the STV-QDs hybridization efficiency; the results demonstrated that it is an accurate nano-scale miRNA quantifier motif. In addition, both symmetrical rectangular motif and asymmetrical China-map motif were tested. With significant linearity in both motifs, our experiments suggested that DNA Origami motif with arbitrary shape can be utilized in this method. Since this DNA origami-based method we developed owns the unique advantages of simple, time-and-material-saving, potentially multi-targets testing in one motif and relatively accurate for certain impurity samples as counted directly by atomic force microscopy rather than fluorescence signal detection, it may be widely used in quantification of miRNAs. |
format | Online Article Text |
id | pubmed-3749204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37492042013-08-29 Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif Zhu, Jie Feng, Xiaolu Lou, Jingyu Li, Weidong Li, Sheng Zhu, Hongxin Yang, Lun Zhang, Aiping He, Lin Li, Can PLoS One Research Article DNA origami is an emerging technology that assembles hundreds of staple strands and one single-strand DNA into certain nanopattern. It has been widely used in various fields including detection of biological molecules such as DNA, RNA and proteins. MicroRNAs (miRNAs) play important roles in post-transcriptional gene repression as well as many other biological processes such as cell growth and differentiation. Alterations of miRNAs' expression contribute to many human diseases. However, it is still a challenge to quantitatively detect miRNAs by origami technology. In this study, we developed a novel approach based on streptavidin and quantum dots binding complex (STV-QDs) labeled single strand displacement reaction on DNA origami to quantitatively detect the concentration of miRNAs. We illustrated a linear relationship between the concentration of an exemplary miRNA as miRNA-133 and the STV-QDs hybridization efficiency; the results demonstrated that it is an accurate nano-scale miRNA quantifier motif. In addition, both symmetrical rectangular motif and asymmetrical China-map motif were tested. With significant linearity in both motifs, our experiments suggested that DNA Origami motif with arbitrary shape can be utilized in this method. Since this DNA origami-based method we developed owns the unique advantages of simple, time-and-material-saving, potentially multi-targets testing in one motif and relatively accurate for certain impurity samples as counted directly by atomic force microscopy rather than fluorescence signal detection, it may be widely used in quantification of miRNAs. Public Library of Science 2013-08-21 /pmc/articles/PMC3749204/ /pubmed/23990889 http://dx.doi.org/10.1371/journal.pone.0069856 Text en © 2013 Zhu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhu, Jie Feng, Xiaolu Lou, Jingyu Li, Weidong Li, Sheng Zhu, Hongxin Yang, Lun Zhang, Aiping He, Lin Li, Can Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif |
title | Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif |
title_full | Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif |
title_fullStr | Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif |
title_full_unstemmed | Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif |
title_short | Accurate Quantification of microRNA via Single Strand Displacement Reaction on DNA Origami Motif |
title_sort | accurate quantification of microrna via single strand displacement reaction on dna origami motif |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749204/ https://www.ncbi.nlm.nih.gov/pubmed/23990889 http://dx.doi.org/10.1371/journal.pone.0069856 |
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