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Two-color imaging of microRNA with enzyme-free signal amplification via hybridization chain reactions in living cells

机译:microRNA的双色成像通过活细胞中的杂交链反应进行无酶信号放大

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摘要

In situ imaging of miRNA in living cells could facilitate the monitoring of the dynamic expression and distribution of miRNA and research on miRNA-related cellular processes and diseases. Given the low expression levels and even down-regulation of cellular miRNA that is associated with some diseases, amplification strategies are imperative for intracellular miRNA imaging. The present paper proposes a non-destructive amplification strategy for use in living cells. This amplification strategy utilizes the enzyme-free hybridization chain reaction (HCR) with graphene oxide (GO) as a carrier to image cellular miRNA. The resulting signal amplification provides excellent recognition and signal enhancement of specific miRNAs in living cells. As the fluorescence quencher and probe carrier, GO enables activation of the signal switch and effective intracellular delivery of amplification reagents. This new imaging method realizes simple, sensitive and non-destructive signal amplification of miRNA in living cells and has an ability to simultaneously image two types of miRNA in the same cell. This method supplies accurate information regarding cellular miRNA-related biological events and provides a new tool for highly sensitive and simultaneous imaging of multiple low-level biomarkers, thereby improving the accuracy of early disease diagnosis.
机译:活细胞中miRNA的原位成像可以促进miRNA的动态表达和分布的监测以及与miRNA相关的细胞过程和疾病的研究。鉴于与某些疾病相关的细胞miRNA的低表达水平甚至下调,扩增策略对于细胞内miRNA成像至关重要。本论文提出了一种用于活细胞的非破坏性扩增策略。这种扩增策略利用无酶杂交链反应(HCR)和氧化石墨烯(GO)作为载体对细胞miRNA进行成像。所得的信号放大可为活细胞中的特定miRNA提供出色的识别和信号增强。作为荧光猝灭剂和探针载体,GO可以激活信号开关并有效地在细胞内递送扩增试剂。这种新的成像方法可实现活细胞中miRNA的简单,灵敏和非破坏性的信号放大,并具有在同一细胞中同时对两种类型的miRNA成像的能力。该方法可提供有关细胞miRNA相关生物学事件的准确信息,并为多种低水平生物标志物的高灵敏度同步成像提供了新工具,从而提高了疾病早期诊断的准确性。

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