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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Label-free cascade amplification strategy for sensitive visual detection of thrombin based on target-triggered hybridization chain reaction-mediated in situ generation of DNAzymes and Pt nanochains
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Label-free cascade amplification strategy for sensitive visual detection of thrombin based on target-triggered hybridization chain reaction-mediated in situ generation of DNAzymes and Pt nanochains

机译:基于目标触发的杂交链反应介导的DNA酶和Pt纳米链原位生成的无标记级联扩增策略,用于凝血酶的灵敏视觉检测

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摘要

A new magnetic bead-based cascade amplification strategy for highly sensitive visual detection of proteins (thrombin as a model analyte) was developed by coupling target-triggered hybridization chain reaction (HCR) with the synergistic catalysis of DNA concatemer-mediated hemin/G-quadruplex DNAzymes and Pt nanozymes. Initially, the biotinylated primer DNA (P-DNA) was complementary with aptamer to form dsDNA which was further linked to streptavidin-coated magnetic bead (MB), thereby fabricating the expected MB-based aptasensor. In the presence of target TB, the aptamer was taken away from the aptasensor, and the free P-DNA immediately triggered HCR to spontaneously form DNA concatemer-directed nanochains with numerous DNAzymes and Pt nanoclusters (PtNCs) to achieve cascades signal amplification. The dual peroxidase mimetics catalyzed the H2O2-mediated oxidation of colorless 3,3',5,5'-tetramethylbenzidine (TMB) into the colored TMB oxides (oxTMB), causing intensified color change of the chromogenic solution for the highly sensitive naked-eye detection of as low as 100.0 pM TB. In this strategy, the employment of magnetic separation and exonuclease III (Exo III)-assisted digestion of residual dsDNA minimized the background noise and avoided the false positive results, greatly improving the detection accuracy and sensitivity with a low limit of detection (LOD=15.0 pM). The proposed visual platform has promise for detecting various types of proteins with careful DNA sequence designs. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过将目标触发的杂交链反应(HCR)与DNA串联体介导的血红素/ G四联体的协同催化偶联,开发了一种新的基于磁珠的级联扩增策略,用于高度灵敏地检测蛋白质(凝血酶作为模型分析物) DNA酶和Pt纳米酶。最初,生物素化的引物DNA(P-DNA)与适体互补形成dsDNA,并进一步与链霉亲和素包被的磁珠(MB)连接,从而制造出了预期的基于MB的适体传感器。在存在目标TB的情况下,将适体从适体传感器上移开,游离的P-DNA立即触发HCR以自发形成具有许多DNA酶和Pt纳米簇(PtNC)的DNA串联体定向的纳米链,以实现级联信号放大。双重过氧化物酶模拟物将H2O2介导的无色3,3',5,5'-四甲基联苯胺(TMB)氧化为有色TMB氧化物(oxTMB),导致高敏感度裸眼发色溶液的颜色变化加剧检测到低至100.0 pM TB。在此策略中,采用磁分离和核酸外切酶III(Exo III)辅助消化残留dsDNA的方法可将背景噪音降至最低,并避免了假阳性结果,从而大大提高了检测准确性和灵敏度,并且检测限较低(LOD = 15.0下午)。拟议的视觉平台有望通过仔细的DNA序列设计检测各种类型的蛋白质。 (C)2016 Elsevier B.V.保留所有权利。

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