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Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase
MicroRNA-21 (miRNA-21) is a significant biomarker which is closely related to some kinds of diseases, such as cancer, cardiovascular disease and kidney disease. Therefore, the detection of miRNA-21 is of great importance and can provide essential information for disease diagnosis. In this study, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050473/ https://www.ncbi.nlm.nih.gov/pubmed/35495318 http://dx.doi.org/10.1039/c9ra10657j |
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author | Huang, Xitong Xu, Zhiming Liu, Ji-Hua Yu, Bo-Yang Tian, Jiangwei |
author_facet | Huang, Xitong Xu, Zhiming Liu, Ji-Hua Yu, Bo-Yang Tian, Jiangwei |
author_sort | Huang, Xitong |
collection | PubMed |
description | MicroRNA-21 (miRNA-21) is a significant biomarker which is closely related to some kinds of diseases, such as cancer, cardiovascular disease and kidney disease. Therefore, the detection of miRNA-21 is of great importance and can provide essential information for disease diagnosis. In this study, we report a facile, sensitive assay for miRNA-21 detection using personal glucose meters (PGM). Biotinylated DNA strand linked invertase (Inv) is conjugated on the surface of streptavidin-coated magnetic beads (MBs) to form a MBs–DNA–Inv complex. Target miRNA-21 in the detection system is captured by the MBs–DNA–Inv probe through DNA/RNA hybridization. The duplex-specific nuclease (DSN) enzyme specifically cleaves the DNA to recycle the target miRNA and release invertase, thereby triggering the dual signal amplification and ensuring high sensitivity. Besides, we establish a linear relationship between PGM and different concentrations of miRNA-21 in the range of 10 to 200 pM. The limit of detection is 1.8 pM, which is more sensitive than some of the previous reports. In addition, the biosensor exhibits excellent sequence selectivity and single-base mutation can be discriminated. Moreover, the expression of miRNA-21 is confirmed in urine from mice by our method, which is in good accordance with the qRT-PCR result. Therefore, a dependable, low-cost strategy for the detection of miRNA has been established and it meets the latest analytical demands for miRNA determination that is suitable for the public. |
format | Online Article Text |
id | pubmed-9050473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90504732022-04-29 Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase Huang, Xitong Xu, Zhiming Liu, Ji-Hua Yu, Bo-Yang Tian, Jiangwei RSC Adv Chemistry MicroRNA-21 (miRNA-21) is a significant biomarker which is closely related to some kinds of diseases, such as cancer, cardiovascular disease and kidney disease. Therefore, the detection of miRNA-21 is of great importance and can provide essential information for disease diagnosis. In this study, we report a facile, sensitive assay for miRNA-21 detection using personal glucose meters (PGM). Biotinylated DNA strand linked invertase (Inv) is conjugated on the surface of streptavidin-coated magnetic beads (MBs) to form a MBs–DNA–Inv complex. Target miRNA-21 in the detection system is captured by the MBs–DNA–Inv probe through DNA/RNA hybridization. The duplex-specific nuclease (DSN) enzyme specifically cleaves the DNA to recycle the target miRNA and release invertase, thereby triggering the dual signal amplification and ensuring high sensitivity. Besides, we establish a linear relationship between PGM and different concentrations of miRNA-21 in the range of 10 to 200 pM. The limit of detection is 1.8 pM, which is more sensitive than some of the previous reports. In addition, the biosensor exhibits excellent sequence selectivity and single-base mutation can be discriminated. Moreover, the expression of miRNA-21 is confirmed in urine from mice by our method, which is in good accordance with the qRT-PCR result. Therefore, a dependable, low-cost strategy for the detection of miRNA has been established and it meets the latest analytical demands for miRNA determination that is suitable for the public. The Royal Society of Chemistry 2020-03-18 /pmc/articles/PMC9050473/ /pubmed/35495318 http://dx.doi.org/10.1039/c9ra10657j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Huang, Xitong Xu, Zhiming Liu, Ji-Hua Yu, Bo-Yang Tian, Jiangwei Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase |
title | Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase |
title_full | Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase |
title_fullStr | Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase |
title_full_unstemmed | Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase |
title_short | Dual signal amplification for microRNA-21 detection based on duplex-specific nuclease and invertase |
title_sort | dual signal amplification for microrna-21 detection based on duplex-specific nuclease and invertase |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050473/ https://www.ncbi.nlm.nih.gov/pubmed/35495318 http://dx.doi.org/10.1039/c9ra10657j |
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