A light-up “G-quadruplex nanostring” for label-free and selective detection of miRNA via duplex-specific nuclease mediated tandem rolling circle amplification

MicroRNA (miRNA) has emerged as a promising genetic marker for cancer diagnosis and therapy because its expression level is closely related to the progression of malignant diseases. Herein, a label-free and selective fluorescence platform was proposed for miRNA based on light-up “G-quadruplex nanost...

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Bibliographic Details
Published inNanomedicine Vol. 32; p. 102339
Main Authors Liu, Li-qi, Yin, Fei, Lu, Yu, Yan, Xi-luan, Wu, Ching-Chou, Li, Xia, Li, Chenzhong
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.02.2021
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Summary:MicroRNA (miRNA) has emerged as a promising genetic marker for cancer diagnosis and therapy because its expression level is closely related to the progression of malignant diseases. Herein, a label-free and selective fluorescence platform was proposed for miRNA based on light-up “G-quadruplex nanostring” via duplex-specific nuclease (DSN) mediated tandem rolling circle amplification (RCA). First, a long DNA generated from upstream RCA was designed with the antisense sequences for miR-21 and downstream RCA primer. Upon recognizing miR-21, the resulting DNA–RNA permitted DSN digestion and triggered downstream two-way RCA, and generation of abundant “G-quadruplex nanostring” binding with ZnPPIX for label-free fluorescent responses. In our strategy, the strong preference of DSN for perfectly matched DNA/RNA ensures its excellent selectivity. The developed method generated wide linear response with LOD of 1.019 fM. Additionally, the miR-21 levels in cell extracts have been evaluated, revealing the utility of this tool for biomedical research and clinical diagnosis. A facile fluorescence detection assay based on a light-up “G-quadruplex nanostring” via duplex specific nuclease mediated tandem rolling circle amplification was proposed for miRNA with powerful label-free signaling reporter, excellent selectivity and enhanced sensitivity in cell extracts, showing a powerful tool for biomedical research and clinical diagnosis. [Display omitted]
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ISSN:1549-9634
1549-9642
DOI:10.1016/j.nano.2020.102339