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二次循环放大法用于 HIV DNA 的无标记和灵敏可视化检测。

Quadratic recycling amplification for label-free and sensitive visual detection of HIV DNA.

机构信息

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Biosens Bioelectron. 2014 May 15;55:220-4. doi: 10.1016/j.bios.2013.12.021. Epub 2013 Dec 16.

Abstract

Visual detections have attracted great research attentions recently due to their convenient monitoring of the target analytes without using any advanced instruments. However, achieving visual detection of trace amounts of biomolecules with PCR-like sensitivity remains a major challenge. In current work, we describe a new quadratic signal amplification strategy for sensitive visual detection of HIV DNA biomarkers based on exonuclease III (Exo III)-assisted DNA recycling amplification and DNAzymes. The presence of the target HIV DNA leads to two independent and simultaneous DNA recycling processes to achieve quadratic signal amplification with the assistance of Exo III. This quadratic signal amplification results in catalytic cleavage of the G-quadruplex sequence-locked hairpin probes to release numerous active G-quadruplex sequences, which further associate with hemin to form DNAzymes and cause significantly intensified color change for sensitive and visual detection of HIV DNA down to 2.5 pM. The proposed visual detection method employs un-modified hairpin DNA as probes, avoids using any complex and expensive instruments for signal transduction and is essentially simple. This method also shows single-base mismatch discrimination capability as well. All these features make our developed DNA detection method holds great potential for visual monitoring of various DNA biomarkers at ultralow levels with careful and proper probe designs.

摘要

由于视觉检测无需使用任何先进仪器即可方便地监测目标分析物,因此最近引起了广泛的研究关注。然而,实现对痕量生物分子进行类似于 PCR 的灵敏视觉检测仍然是一个主要挑战。在当前的工作中,我们描述了一种新的二次信号放大策略,用于基于外切酶 III(Exo III)辅助的 DNA 循环扩增和 DNA 酶灵敏可视化检测 HIV DNA 生物标志物。目标 HIV DNA 的存在导致两个独立且同时的 DNA 循环过程,在外切酶 III 的辅助下实现二次信号放大。这种二次信号放大导致 G-四链体序列锁扣发夹探针的催化裂解,释放出大量活性 G-四链体序列,进一步与血红素结合形成 DNA 酶,并导致 HIV DNA 的灵敏和可视化检测发生显著的颜色变化,检测下限低至 2.5 pM。所提出的视觉检测方法采用未经修饰的发夹 DNA 作为探针,避免使用任何复杂且昂贵的仪器进行信号转导,本质上非常简单。该方法还具有单碱基错配识别能力。所有这些特性使得我们开发的 DNA 检测方法在经过仔细和适当的探针设计后,具有在超低水平下对各种 DNA 生物标志物进行可视化监测的巨大潜力。

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