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首页> 外文期刊>Analytica chimica acta >MnO2 nanosheet-mediated ratiometric fluorescence biosensor for MicroRNA detection and imaging in living cells
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MnO2 nanosheet-mediated ratiometric fluorescence biosensor for MicroRNA detection and imaging in living cells

机译:MnO2纳米型介导的比例荧光生物传感器,用于微小RNA检测和活细胞成像

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MicroRNA (miRNA) plays significant roles in cell proliferation, differentiation and apoptosis, and has been considered to be valuable biomarker for cancer. Accurate and sensitive detection of miRNA is crucially significant for cancer diagnosis and treatment. Here, a MnO2 nanosheet-mediated ratiometric fluorescence biosensor was designed for miRNA detection and imaging in living cells. It contained MnO2 nanosheets acting as DNA carrier, and fluorescent donor (FAM)-labeled hairpin H1 (recognition probe) and fluorescent acceptor (TAMRA)-labeled hairpin H2 (amplification probe). When the biosensor entered cell by endocytosis, MnO2 nanosheets were degraded to Mn2+ via intracellular glutathione (GSH) and the adsorbed hairpins H1 and H2 were released. The intracellular target miRNA-21 hybridized with the recognition unit of H1 to initiate catalyzed hairpin assembly (CHA) and a large amount of H1-H2 duplexes were produced. This brought fluorescent donor FAM and fluorescent acceptor TAMRA into close proximity to produce fluorescence resonance energy transfer (FRET), inducing a ratiometric fluorescent response (donor signal decreased and acceptor signal enhanced) for miRNA-21 detection. Furthermore, this method could be applied to differentiate the expression levels of miRNA-21 in HeLa, HepG-2 and L02 cells. These results indicated that the proposed method possessed great potential in the early diagnosis of miRNA-related diseases. (C) 2019 Elsevier B.V. All rights reserved.
机译:microRNA(miRNA)在细胞增殖,分化和细胞凋亡中起着显着的作用,并且被认为是癌症的有价值的生物标志物。对miRNA的准确和灵敏的检测对于癌症诊断和治疗至关重要。这里,设计了MnO2纳米型介导的比例荧光生物传感器,用于在活细胞中进行miRNA检测和成像。它含有用作DNA载体的MNO2纳米片,荧光供体(FAM) - 标记的发夹H1(识别探针)和荧光受体(TAMRA) - 标记发夹H2(扩增探针)。当生物传感器通过内吞作用进入细胞时,MNO2纳米片通过细胞内谷胱甘肽(GSH)降解到MN2 +,并且释放吸附的发夹H1和H 2。产生与H1识别单元杂交以引发催化的发夹组合物(CHA)和大量H1-H2双链体的细胞内靶靶MiRNA-21。这将荧光供体FAM和荧光受体TAMRA紧密地接近,以产生荧光共振能量转移(FRET),诱导MIRNA-21检测的比率荧光响应(供体信号减少和受体信号增强)。此外,可以应用该方法以将MiRNA-21的表达水平分化为HeLa,HepG-2和L02细胞中的miRNA-21。这些结果表明,该方法在与MiRNA相关疾病的早期诊断中具有巨大潜力。 (c)2019年Elsevier B.V.保留所有权利。

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