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Ultrasensitive fluorescence detection of sequence-specific DNA via labeling hairpin DNA probes for fluorescein o-acrylate polymers

机译:通过标记发夹DNA探针对荧光素O-丙烯酸酯聚合物的超敏荧光检测序列特异性DNA

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Sensitive detection of DNA is conducive to enhance the accuracy of diseases diagnosis and risk prediction. In this work, we report the use of activators generated by electron transfer for atom transfer radical polymerization (AGET ATRP) as a novel on-chip amplification strategy for the fluorescence detection of DNA. More specifically, the target DNA was captured by the on-chip immobilized hairpin DNA probes. Upon hybridization, exposed 3'-N-3 of the hairpin was used to attach AGET ATRP initiators onto the silicon surface by click chemistry. Then, numerous fluorescent labeling linked to the end of the probes via the formation of long chain polymers of fluorescein o-acrylate, which in turn amplified the fluorescence signal for DNA detection. Under optimal conditions, it showed a good linear range from 100 fM to 1 mu M in DNA detection, with the limit of detection as low as 4.3 fM. Moreover, this strategy showed good detection performance in complex real serum samples, the fluorescence intensity of 0.1 nM tDNA in 1% fetal bovine serum samples was 97.6% of that in Tris-EDTA buffer. Based on its high sensitivity, reduced cost and simplicity, the proposed signal amplification strategy displays translational potential in clinical application. (C) 2019 Elsevier B.V. All rights reserved.
机译:DNA的敏感性检测有利于提高疾病诊断和风险预测的准确性。在这项工作中,我们报告了使用通过电子转移产生的激活剂,用于原子转移自由基聚合(Aget ATRP)作为用于DNA荧光检测的新型片上放大策略。更具体地,通过片上固定的发夹探针捕获靶DNA。在杂交后,使用暴露的3'-n-3用点击化学将Aget ATRP引发剂附着到硅表面上。然后,许多荧光标记通过形成荧光素O-丙烯酸酯的长链聚合物连接到探针的末端,其又扩增荧光信号进行DNA检测。在最佳条件下,它在DNA检测中显示出100 fm至1μm的良好线性范围,检测限为低至4.3 fm。此外,该策略在复杂的真实血清样品中显示出良好的检测性能,1%胎牛血清样品中0.1nm TDNA的荧光强度为TRIS-EDTA缓冲液中的97.6%。基于其高灵敏度,降低成本和简单性,所提出的信号放大策略显示临床应用中的平移潜力。 (c)2019年Elsevier B.V.保留所有权利。

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