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

机译:MicroRNA的双色成像与酶无信号扩增通过活细胞中的杂交链反应

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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:原位活细胞中miRNA的成像可以促进MiRNA的动态表达和分布和对miRNA相关细胞过程和疾病的研究。鉴于与某些疾病相关的细胞miRNA的低表达水平甚至降低调节,扩增策略对于细胞内miRNA成像是必不可少的。本文提出了用于活细胞的非破坏性扩增策略。该扩增策略利用酶无杂交链反应(HCR)用石墨烯(GO)作为图像细胞miRNA的载体。所得到的信号放大提供活细胞中特定miRNA的优异识别和信号增强。作为荧光猝灭剂和探针载体,GO使能信号开关的激活和扩增试剂的有效细胞内递送。这种新的成像方法实现了活细胞中miRNA的简单,敏感性和非破坏性的信号放大,并且能够在同一细胞中同时进行两种类型的miRNA。该方法提供有关细胞miRNA相关的生物事件的准确信息,并为多个低级生物标志物的高度敏感和同时成像提供新的工具,从而提高了早期疾病诊断的准确性。

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