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Biosensing Amplification by Hybridization Chain Reaction on Phase-Sensitive Surface Plasmon Resonance

机译:相敏表面等离子体共振杂交链反应的生物沉积扩增

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摘要

Surface Plasmon Resonance (SPR) is widely used in biological and chemical sensing with fascinating properties. However, the application of SPR to detect trace targets is hampered by non-specific binding and poor signal. A variety of approaches for amplification have been explored to overcome this deficiency including DNA aptamers as versatile target detection tools. Hybridization chain reaction (HCR) is a high-efficiency enzyme-free DNA amplification method operated at room temperature, in which two stable species of DNA hairpins coexist in solution until the introduction of the initiator strand triggers a cascade of hybridization events. At an optimal salt condition, as the concentrations of H1 and H2 increased, the HCR signals were enhanced, leading to signal amplification reaching up to 6.5-fold of the detection measure at 30 min. This feature enables DNA to act as an amplifying transducer for biosensing applications to provide an enzyme-free alternative that can easily detect complex DNA sequences. Improvement of more diverse recognition events can be achieved by integrating HCR with a phase-sensitive SPR (pSPR)-tested aptamer stimulus. This work seeks to establish pSPR aptamer system for highly informative sensing by means of an amplification HCR. Thus, combining pSPR and HCR technologies provide an expandable platform for sensitive biosensing.
机译:表面等离子体共振(SPR)广泛用于生物和化学感测,具有迷人的特性。然而,通过非特异性结合和差的信号阻碍了SPR检测迹线目标的应用。已经探索了各种扩增方法以克服这种缺陷,包括DNA适体作为多功能目标检测工具。杂交链反应(HCR)是在室温下操作的高效酶的DNA扩增方法,其中两个稳定的DNA发夹在溶液中共存,直至引入引发剂股线触发杂交事件的级联。在最佳盐条件下,随着H1和H2的浓度增加,HCR信号得到增强,导致信号放大在30分钟内达到6.5倍的检测措施。该特征使DNA能够充当用于生物传感器应用的放大换能器,以提供可以容易地检测复杂DNA序列的无酶替代品。通过将HCR与相敏感SPR(PSPR)溶液(PSPR)溶液集成,可以实现更多样化的识别事件的改进。这项工作旨在通过扩增HCR建立PSPR适体系统以获得高度信息性的感测。因此,组合PSPR和HCR技术为敏感的生物传感提供可扩展平台。

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