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在金属表面进行杂交链反应作为 SPR 和电化学生物传感器中信号放大的一种手段。

Hybridization chain reaction performed on a metal surface as a means of signal amplification in SPR and electrochemical biosensors.

机构信息

Institute of Bioengineering at the Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

Department of Electronics Technology at the Budapest University of Technology and Economics, Budapest, Hungary.

出版信息

Biosens Bioelectron. 2014 Apr 15;54:102-8. doi: 10.1016/j.bios.2013.10.036. Epub 2013 Oct 31.

Abstract

A more specific and intense signal is desirable for most kinds of biosensors for biomedical or environmental applications, and it is especially so for label-free biosensors. In this paper, we show that hybridization chain reaction (HCR) can be exploited for the easily detectable accumulation of nucleic acids on metal surfaces as an event triggered by specific recognition between a probe and a target nucleic acid. We show that this process could be exploited to increase the sensitivity in the detection of nucleic acids derived from a pathogenic microorganism. This strategy can be straightforwardly implemented on SPR biosensors (commercial or custom-built) or on label-free electrochemical biosensors. Together with signal amplification, HCR can serve as a confirmation of the specificity of target recognition, as it involves the specific matching with a separate base sequence in the target nucleic acid. Furthermore, the kinetics of the target binding and the HCR can be easily distinguished from each other, providing an additional means of confirmation of the specific recognition.

摘要

对于大多数用于生物医学或环境应用的生物传感器来说,更具体和强烈的信号是理想的,对于无标记生物传感器尤其如此。在本文中,我们表明杂交链式反应 (HCR) 可用于在金属表面上容易检测到的核酸积累,作为探针和靶核酸之间特定识别触发的事件。我们表明,该过程可用于提高源自致病微生物的核酸检测的灵敏度。该策略可以直接在 SPR 生物传感器(商业或定制)或无标记电化学生物传感器上实施。与信号放大相结合,HCR 可以作为靶识别特异性的确认,因为它涉及与靶核酸中的单独碱基序列的特异性匹配。此外,目标结合的动力学和 HCR 可以很容易地彼此区分,提供了特异性识别的另一种确认手段。

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