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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Establishment of a universal and sensitive plasmonic biosensor platform based on the hybridization chain reaction (HCR) amplification induced by a triple-helix molecular switch
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Establishment of a universal and sensitive plasmonic biosensor platform based on the hybridization chain reaction (HCR) amplification induced by a triple-helix molecular switch

机译:基于三螺旋分子开关诱导的杂交链反应(HCR)扩增的普遍敏感等离子感植物平台的建立

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Herein, we established a universal and sensitive plasmonic sensing strategy for biomolecule assays by coupling the hybridization chain reaction (HCR) strategy and a triple-helix molecular switch. Upon the recognition of the target, a single-stranded DNA as a universal trigger (UT) was released from the triplehelix molecular switch (THMS). Thus, the HCR process can be triggered between two hairpins M1 and M2, resulting in the aggregation of gold nanoparticles (AuNPs) via the hybridization between the tail sequence on M1 (or M2) and a DNA-AuNP probe with a dramatic change in the absorbance at 521 nm. More specifically, the strategy, which was conducted by the introduction of target-specific recognition of THMS and universalized by virtue of altering the aptamer or DNA sequence without changing the triplehelix structure, enables simple design for multiple target detection. By taking advantage of THMS, this strategy could enable stable and sensitive detection of a variety of targets including nucleic acids, small molecules and proteins, which may possess great potential for practical applications.
机译:在此,我们通过偶联杂交链反应(HCR)策略和三螺旋分子开关,建立了用于生物分子测定的普遍和敏感的等离子体传感策略。在识别靶时,从Triplehelix分子开关(THM)中释放单链DNA作为通用触发(UT)。因此,HCR方法可以在两个发夹M1和M2之间触发,导致金纳米颗粒(AUNP)聚集在M1(或M2)上的尾序列之间的杂交和具有剧烈变化的DNA-AUNP探针之间的杂交吸光度为521纳米。更具体地说,通过引入目标特异性识别和通过改变适体或DNA序列而不改变Triplehelix结构的局部识别来进行的策略,使得能够简单地设计多个目标检测。通过利用THM,该策略可以稳定和敏感地检测各种靶标,包括核酸,小分子和蛋白质,这可能对实际应用具有巨大潜力。

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