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Quantitative and multiplexed microRNA sensing in living cells based on peptide nucleic acid and nano graphene oxide (PANGO)

机译:基于肽核酸和纳米氧化石墨烯(PANGO)的活细胞中的定量和多重microRNA传感

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摘要

MicroRNA (miRNA) is an important small RNA which regulates diverse gene expression at the post-transcriptional level. miRNAs are considered as important biomarkers since abnormal expression of specific miRNAs is associated with many diseases including cancer and diabetes. Therefore, it is important to develop biosensors to quantitatively detect miRNA expression levels. Here, we develop a nanosized graphene oxide (NGO) based miRNA sensor, which allows quantitative monitoring of target miRNA expression levels in living cells. The strategy is based on tight binding of NGO with peptide nucleic acid (PNA) probes, resulting in fluorescence quenching of the dye that is conjugated to the PNA, and subsequent recovery of the fluorescence upon addition of target miRNA. PNA as a probe for miRNA sensing offers many advantages including high sequence specificity, high loading capacity on the NGO surface compared to DNA and resistance against nuclease-mediated degradation. The present miRNA sensor allowed the detection of specific target miRNAs with the detection limit as low as ~1 pM and the simultaneous monitoring of three different miRNAs in a living cell.
机译:MicroRNA(miRNA)是一种重要的小RNA,可在转录后水平调控多种基因的表达。 miRNA被认为是重要的生物标志物,因为特定miRNA的异常表达与包括癌症和糖尿病在内的许多疾病有关。因此,开发生物传感器以定量检测miRNA表达水平非常重要。在这里,我们开发了一种基于纳米石墨烯(NGO)的miRNA传感器,该传感器可以定量监测活细胞中目标miRNA的表达水平。该策略基于NGO与肽核酸(PNA)探针的紧密结合,从而导致与PNA偶联的染料发生荧光猝灭,并在添加目标miRNA后恢复荧光。 PNA作为miRNA传感的探针具有许多优势,包括与DNA相比具有高序列特异性,在NGO表面上的高负载能力以及对核酸酶介导的降解的抵抗力。目前的miRNA传感器允许检测特定目标的miRNA,检测限低至〜1 pM,并且可以同时监测活细胞中的三种不同的miRNA。

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