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A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
Nowadays a variety of biosensors are widely used in different fields, including biomedical diagnostics and self-testing. Nucleic acid-based biosensors are typically applied to detect another nucleic acid, proteins, ions, and several other types of compounds. It is most promising to develop simple an...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277777/ https://www.ncbi.nlm.nih.gov/pubmed/32550928 http://dx.doi.org/10.3762/bjoc.16.100 |
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author | Bryushkova, Ekaterina Alexandrovna Gandalipov, Erik Rafikovich Nuzhina, Julia Victorovna |
author_facet | Bryushkova, Ekaterina Alexandrovna Gandalipov, Erik Rafikovich Nuzhina, Julia Victorovna |
author_sort | Bryushkova, Ekaterina Alexandrovna |
collection | PubMed |
description | Nowadays a variety of biosensors are widely used in different fields, including biomedical diagnostics and self-testing. Nucleic acid-based biosensors are typically applied to detect another nucleic acid, proteins, ions, and several other types of compounds. It is most promising to develop simple and effective biosensors for the use in situations where traditional methods are not available due to their complexity and laboriousness. In this project, a novel smart deoxyribozyme-based fluorescent sensor for the detection of androgen receptor mRNA was developed. It consists of several functional modules including two deoxyribozymes 10–23, an RNA-dependent split malachite green aptamer, and an oligonucleotide platform. Deoxyribozymes specifically release a 27-nucleotide RNA fragment that is readily available for the interaction with the aptamer module. This solves a problem of secondary structure in hybridization with the target sequence of full-length mRNA. It was shown that within 24 hours the proposed sensor specifically recognized both a synthetic 60-nucleotide RNA fragment (LOD is 1.4 nM of RNA fragment at 37 °C) and a full-sized mRNA molecule of the androgen receptor. The constructed sensor is easy to use, has high efficiency and selectivity for the RNA target, and can be reconstructed for the detection of various nucleic acid sequences due to its modular structure. Thus, similar biosensors may be useful for the differential diagnosis. |
format | Online Article Text |
id | pubmed-7277777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-72777772020-06-17 A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA Bryushkova, Ekaterina Alexandrovna Gandalipov, Erik Rafikovich Nuzhina, Julia Victorovna Beilstein J Org Chem Full Research Paper Nowadays a variety of biosensors are widely used in different fields, including biomedical diagnostics and self-testing. Nucleic acid-based biosensors are typically applied to detect another nucleic acid, proteins, ions, and several other types of compounds. It is most promising to develop simple and effective biosensors for the use in situations where traditional methods are not available due to their complexity and laboriousness. In this project, a novel smart deoxyribozyme-based fluorescent sensor for the detection of androgen receptor mRNA was developed. It consists of several functional modules including two deoxyribozymes 10–23, an RNA-dependent split malachite green aptamer, and an oligonucleotide platform. Deoxyribozymes specifically release a 27-nucleotide RNA fragment that is readily available for the interaction with the aptamer module. This solves a problem of secondary structure in hybridization with the target sequence of full-length mRNA. It was shown that within 24 hours the proposed sensor specifically recognized both a synthetic 60-nucleotide RNA fragment (LOD is 1.4 nM of RNA fragment at 37 °C) and a full-sized mRNA molecule of the androgen receptor. The constructed sensor is easy to use, has high efficiency and selectivity for the RNA target, and can be reconstructed for the detection of various nucleic acid sequences due to its modular structure. Thus, similar biosensors may be useful for the differential diagnosis. Beilstein-Institut 2020-05-27 /pmc/articles/PMC7277777/ /pubmed/32550928 http://dx.doi.org/10.3762/bjoc.16.100 Text en Copyright © 2020, Bryushkova et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Bryushkova, Ekaterina Alexandrovna Gandalipov, Erik Rafikovich Nuzhina, Julia Victorovna A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA |
title | A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA |
title_full | A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA |
title_fullStr | A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA |
title_full_unstemmed | A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA |
title_short | A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA |
title_sort | smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mrna |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277777/ https://www.ncbi.nlm.nih.gov/pubmed/32550928 http://dx.doi.org/10.3762/bjoc.16.100 |
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