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Aptamer-based and DNAzyme-linked colorimetric detection of cancer cells

机译:基于适体和DNAzyme的比色法检测癌细胞

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摘要

This paper reports a novel method to detect human leukemic lymphoblasts (CCRF-CEM cells). While the aptamer of the cancer cells was employed as the recognition element to target cancer cells, peroxidaseactive DNAzyme was used as the sensing element to produce catalysis-induced colorimetric signals. The elegant architecture integrating the aptamer and DNAzyme made it feasible to detect cancer cells easily and rapidly by the color change of the substrate for DNAzyme. Experimental results showed that 500 cells can well indicate the cancer, while as control, 250,000 Islet Island Beta cells only show tiny signals, suggesting that the method proposed in this paper has considerable sensitivity and selectivity. Furthermore, since it does not require expensive apparatus, or modification or label of DNA chains, the method we present here is also cost-effective and conveniently operated, implying potential applications in future cancer diagnosis.
机译:本文报道了一种检测人白血病淋巴母细胞(CCRF-CEM细胞)的新方法。当癌细胞的适体被用作靶向癌细胞的识别元件时,过氧化物酶活性的DNAzyme被用作感测元件,以产生催化诱导的比色信号。结合了适体和DNAzyme的优雅架构使通过DNAzyme底物的颜色变化轻松,快速地检测癌细胞成为可能。实验结果表明,有500个细胞可以很好地预示癌症,而作为对照的25万个Islet Island Beta细胞仅显示微小信号,这表明本文提出的方法具有相当高的灵敏度和选择性。此外,由于不需要昂贵的设备或DNA链的修饰或标记,因此我们在此提出的方法也是经济高效且操作简便的,这暗示了在未来癌症诊断中的潜在应用。

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