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基于巯基功能化碳点通过靶标引发的血红素/ G-四链体催化氧化实现的无标记和无酶荧光检测微小RNA

Label-free and enzyme-free fluorescence detection of microRNA based on sulfydryl-functionalized carbon dots via target-initiated hemin/G-quadruplex-catalyzed oxidation.

作者信息

Chen Jianling, Yan Ji, Feng Qiumei, Miao Xiangmin, Dou Baoting, Wang Po

机构信息

School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, China; School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.

School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, China.

出版信息

Biosens Bioelectron. 2021 Mar 15;176:112955. doi: 10.1016/j.bios.2020.112955. Epub 2021 Jan 1.

DOI:10.1016/j.bios.2020.112955
PMID:33412427
Abstract

Carbon dots (CDs)-based biosensors have attracted considerable interest in reliable and sensitive detection of microRNA (miRNA) because of their merits of ultra-small size, excellent biosafety and tunable emission, whereas complicated labeling procedure and expensive bioenzyme associated with current strategies significantly limit their practical application. Herein, we developed a label-free and enzyme-free fluorescence strategy based on strand displaced amplification (SDA) for highly sensitive detection of miRNA using sulfydryl-functionalized CDs (CDs-SH) as probe. CDs-SH displayed excellent response to G-quadruplex DNA against other DNAs based on based on the catalytic oxidation of -SH into -S-S- by hemin/G-quadruplex. Further, CDs-SH were employed to detect miRNA, using miRNA-21 as target model, which triggered the SDA reaction of P1 and P2 to generate hemin/G-quadruplex, subsequently making CDs-SH transform from dot to aggresome along with the quenched fluorescence. Therefore, label-free, enzyme-free, and highly sensitive analysis of miRNA-21 was readily acquired with a limit of detection at 0.03 pM. This proposed biosensor couples the advantages of CDs and label-free/enzyme-free strategy, and thus has a significant potential to be used in early and accurate diagnosis of cancer.

摘要

基于碳点(CDs)的生物传感器因其超小尺寸、出色的生物安全性和可调节发射等优点,在可靠且灵敏地检测微小RNA(miRNA)方面引起了广泛关注。然而,当前策略中复杂的标记程序和昂贵的生物酶显著限制了它们的实际应用。在此,我们开发了一种基于链置换扩增(SDA)的无标记、无酶荧光策略,用于使用巯基功能化碳点(CDs-SH)作为探针高灵敏地检测miRNA。基于血红素/ G-四链体将-SH催化氧化为-S-S-,CDs-SH对G-四链体DNA相对于其他DNA表现出优异的响应。此外,以miRNA-21作为靶标模型,利用CDs-SH检测miRNA,这触发了P1和P2的SDA反应以生成血红素/ G-四链体,随后使CDs-SH从点转变为聚集体,同时荧光猝灭。因此,能够轻松实现对miRNA-21的无标记、无酶且高灵敏分析,检测限低至0.03 pM。这种提出的生物传感器结合了CDs以及无标记/无酶策略的优点,因此在癌症的早期准确诊断中具有巨大的应用潜力。

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