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Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
Biomolecular self-assembly has spurred substantial research efforts for the development of low-cost point-of-care diagnostics. Herein, we introduce an isothermal enzyme-free concatenated hybridization chain reaction (C-HCR), in which the output of the upstream hybridization chain reaction (HCR-1) la...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869291/ https://www.ncbi.nlm.nih.gov/pubmed/29629073 http://dx.doi.org/10.1039/c7sc03939e |
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author | Wei, Jie Gong, Xue Wang, Qing Pan, Min Liu, Xiaoqing Liu, Jing Xia, Fan Wang, Fuan |
author_facet | Wei, Jie Gong, Xue Wang, Qing Pan, Min Liu, Xiaoqing Liu, Jing Xia, Fan Wang, Fuan |
author_sort | Wei, Jie |
collection | PubMed |
description | Biomolecular self-assembly has spurred substantial research efforts for the development of low-cost point-of-care diagnostics. Herein, we introduce an isothermal enzyme-free concatenated hybridization chain reaction (C-HCR), in which the output of the upstream hybridization chain reaction (HCR-1) layer acts as an intermediate input to activate the downstream hybridization chain reaction (HCR-2) layer. The initiator motivates HCR-1 through the autonomous cross-opening of two functional DNA hairpins, yielding polymeric dsDNA nanowires composed of numerous tandem triggers T as output of the primary sensing event. The reconstituted amplicon T then initiates HCR-2 and transduces the analyte recognition into an amplified readout, originating from the synergistic effect between HCR-1 and HCR-2 layers. Native gel electrophoresis, atom force microscopy (AFM) and fluorescence spectra revealed that C-HCR mediated the formation of frond-like branched dsDNA nanowires and the generation of an amplified FRET signal. As a versatile and robust amplification strategy, the unpreceded C-HCR can discriminate DNA analyte from its mutants with high accuracy and specificity. By incorporating an auxiliary sensing module, the integrated C-HCR amplifier was further adapted for highly sensitive and selective detection of microRNA (miRNA), as a result of the hierarchical and sequential hybridization chain reactions, in human serum and even living cells through an easy-to-integrate “plug-and-play” procedure. In addition, the C-HCR amplifier was successfully implemented for intracellular miRNA imaging by acquiring an accurate and precise signal localization inside living cells, which was especially suitable for the ex situ and in situ amplified detection of trace amounts of analyte. The C-HCR amplification provides a comprehensive and smart toolbox for highly sensitive detection of various biomarkers and thus should hold great promise in clinical diagnosis and assessment. The infinite layer of multilayered C-HCR is anticipated to further strengthen the amplification capacity and reliability (anti-invasion performance) of intracellular imaging approach, which is of great significance for its bioanalytical applications. |
format | Online Article Text |
id | pubmed-5869291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-58692912018-04-06 Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging Wei, Jie Gong, Xue Wang, Qing Pan, Min Liu, Xiaoqing Liu, Jing Xia, Fan Wang, Fuan Chem Sci Chemistry Biomolecular self-assembly has spurred substantial research efforts for the development of low-cost point-of-care diagnostics. Herein, we introduce an isothermal enzyme-free concatenated hybridization chain reaction (C-HCR), in which the output of the upstream hybridization chain reaction (HCR-1) layer acts as an intermediate input to activate the downstream hybridization chain reaction (HCR-2) layer. The initiator motivates HCR-1 through the autonomous cross-opening of two functional DNA hairpins, yielding polymeric dsDNA nanowires composed of numerous tandem triggers T as output of the primary sensing event. The reconstituted amplicon T then initiates HCR-2 and transduces the analyte recognition into an amplified readout, originating from the synergistic effect between HCR-1 and HCR-2 layers. Native gel electrophoresis, atom force microscopy (AFM) and fluorescence spectra revealed that C-HCR mediated the formation of frond-like branched dsDNA nanowires and the generation of an amplified FRET signal. As a versatile and robust amplification strategy, the unpreceded C-HCR can discriminate DNA analyte from its mutants with high accuracy and specificity. By incorporating an auxiliary sensing module, the integrated C-HCR amplifier was further adapted for highly sensitive and selective detection of microRNA (miRNA), as a result of the hierarchical and sequential hybridization chain reactions, in human serum and even living cells through an easy-to-integrate “plug-and-play” procedure. In addition, the C-HCR amplifier was successfully implemented for intracellular miRNA imaging by acquiring an accurate and precise signal localization inside living cells, which was especially suitable for the ex situ and in situ amplified detection of trace amounts of analyte. The C-HCR amplification provides a comprehensive and smart toolbox for highly sensitive detection of various biomarkers and thus should hold great promise in clinical diagnosis and assessment. The infinite layer of multilayered C-HCR is anticipated to further strengthen the amplification capacity and reliability (anti-invasion performance) of intracellular imaging approach, which is of great significance for its bioanalytical applications. Royal Society of Chemistry 2017-10-23 /pmc/articles/PMC5869291/ /pubmed/29629073 http://dx.doi.org/10.1039/c7sc03939e Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Wei, Jie Gong, Xue Wang, Qing Pan, Min Liu, Xiaoqing Liu, Jing Xia, Fan Wang, Fuan Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging |
title | Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
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title_full | Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
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title_fullStr | Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
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title_full_unstemmed | Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
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title_short | Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
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title_sort | construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869291/ https://www.ncbi.nlm.nih.gov/pubmed/29629073 http://dx.doi.org/10.1039/c7sc03939e |
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