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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...

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Autores principales: Wei, Jie, Gong, Xue, Wang, Qing, Pan, Min, Liu, Xiaoqing, Liu, Jing, Xia, Fan, Wang, Fuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
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.
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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
title_full Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
title_fullStr Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
title_full_unstemmed Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
title_short Construction of an autonomously concatenated hybridization chain reaction for signal amplification and intracellular imaging
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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