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首页> 外文期刊>Sensors and Actuators >Novel multiple strand displacement reaction coupled hybridization chain reaction for label-free and ultrasensitive electrochemical Type b3a2 biosensing
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Novel multiple strand displacement reaction coupled hybridization chain reaction for label-free and ultrasensitive electrochemical Type b3a2 biosensing

机译:新型多链位移反应耦合杂交链反应,用于无敏感电化学型B3A2生物溶解

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摘要

Herein, a novel simple multiple strand displacement reaction (MSDR) coupled hybridization strand reaction (HCR) was proposed for label-free and ultrasensitive Type b3a2 assay. First, two kinds of messenger DNAs (mDNAs) were aligned on a long substrate strand DNA, which was immobilized on magnetic beads. Unlike traditional SDR, in the presence of target and a hairpin DNA, MSDR would be initiated and achieve target-recycling as well as the release of two mDNAs. Finally, one target input can convert into multiple mDNAs, which greatly increased the utility ratio of target. After magnetic separation, the released mDNAs can hybridize with the hairpin DNA immobilized on the electrode to trigger HCR and form a linear duplex-DNA structure. It can be used as an excellent template to in-situ grown silver nanoparticles (AgNPs) to generate electrochemical response directly. By taking advantage of MSDR as well as HCR, the electrochemical signal was amplified significantly. Under optimal conditions, this developed biosensor achieved a low detection limit of 0.56 fM (S/ N = 3) and a wide linear range from 10 fM to 10 nM for sensitive detection of Type b3a2 with good selectivity and stability.
机译:在此,提出了一种新型简单的多链位移反应(MSDR)偶联杂交链反应(HCR),用于无标记和超敏感型B3A2测定。首先,两种信使DNA(MDNA)在长衬底链DNA上对准,该DNA固定在磁珠上。与传统SDR不同,在靶标和发夹DNA存在下,MSDR将被启动并实现目标回收以及两个MDNA的释放。最后,一个目标输入可以转换为多个MDNA,这大大提高了目标的公用设量比。在磁性分离后,释放的MDNA可以与固定在电极上的发夹DNA杂交以触发HCR并形成线性双链DNA结构。它可以用作原位生长的银纳米颗粒(AgNP)的优异模板,直接产生电化学响应。通过利用MSDR以及HCR,电化学信号显着扩增。在最佳条件下,该开发的生物传感器达到0.56 fm(s / n = 3)的低检测限,宽线性范围为10 fm至10nm,用于良好的选择性和稳定性的B3A2型型B3A2。

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