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Selective and sensitive detection of chronic myeloid leukemia using fluorogenic DNAzyme probes

机译:使用荧光DNAzyme探针的选择性和敏感检测慢性骨髓白血病

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One of the major challenges facing the early diagnosis of chronic myelogenous leukemia (CML) patients today is enhancing the simplicity, rapidness, sensitivity and specificity of detection assay for easy clinical implementation. RNA-cleaving fluorogenic DNAzymes (RFDs) are single-stranded DNA molecules with catalytic activity and can produce fluorescent signals when combined with specific targets. As K562 cells were the first established human immortalized myelogenous leukemia line, we try to screen several RFDs using the crude extracellular mixture of K562 cells through the SELEX process. We obtained an RFD probe A1-3 that is able to distinguish K562 cells from other tumor cell lines. 10 nM of A1-3 can induce an increase of detectable fluorescence signal. Moreover, the RFD assay system can work well for target detection in complex serum matrix. The optimized RFD assay system with low cost also has a desirable ability to exactly distinguish K562 cells after truncation of 20 bases in the 5'end of A1-3. This study is the first report to investigate the RFD system for detection of K562 cells using cell culture supernatants as the complex target. This RFD assay system could potentially be applied for the diagnosis of CML. (C) 2020 Elsevier B.V. All rights reserved.
机译:目前慢性髓性白血病(CML)患者早期诊断的主要挑战之一是提高检测试验的简单性,快速,敏感性和特异性,以便于临床实施。 RNA切割荧光二氮杂体(RFD)是具有催化活性的单链DNA分子,并且在与特定靶标结合时可以产生荧光信号。由于K562细胞是第一个已建立的人造永生化的髓性白血病系列,我们尝试通过SELEX方法使用K562细胞的粗细胞外混合物筛选几个RFD。我们获得了能够将K562细胞与其他肿瘤细胞系区分开的RFD探针A1-3。 A1-3的10nm可以诱导可检测荧光信号的增加。此外,RFD测定系统可以很好地适用于复合血清基质中的目标检测。具有低成本的优化RFD测定系统还具有所需的能力,可以在A1-3的5'突出20个碱基后完全区分K562细胞。该研究是研究RFD系统用于使用细胞培养上清液作为复合靶检测K562细胞的RFD系统的报告。该RFD测定系统可能适用于CML的诊断。 (c)2020 Elsevier B.V.保留所有权利。

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