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基于微粒子在组合声-重力场中从玻璃平板上解离的皮摩尔 DNA 检测。

Zeptomole detection of DNA based on microparticle dissociation from a glass plate in a combined acoustic-gravitational field.

机构信息

Department of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8571, Japan.

Department of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8571, Japan.

出版信息

Talanta. 2022 Feb 1;238(Pt 2):123042. doi: 10.1016/j.talanta.2021.123042. Epub 2021 Nov 6.

Abstract

In this study, we propose a novel detection principle based on the dissociation of microparticles immobilized on a glass plate through weak hybridization involving 4-6 base pairs (bps) in a combined acoustic-gravitational field. Particle dissociation from the glass plate occurs when the resultant of the acoustic radiation force (F) and the sedimentation force (F) exerted on the particle exceeds the binding force owing to the weak hybridization (F). Because F and F can be controlled by the microparticle density, and F is a function of the applied voltage to the transducer (V), an increase in V induces particle dissociation. The binding of gold nanoparticles (AuNPs) onto silica microparticles (SPs) resulting from the strong hybridization of 20 bps induces an increase in the density of SPs, leading to an increase in F and F; consequently, the voltage V required for dissociation becomes lower than that required without AuNP binding. We demonstrate that the dependence of the binding number of AuNPs per SP on V follows the theoretical prediction. The binding of 7500 AuNPs per SP can be detected as a 10 V change in V. The present approach allows the detection of 2000 DNA molecules involved in the strong hybridization between AuNPs and SP.

摘要

在这项研究中,我们提出了一种新的检测原理,该原理基于在组合声 - 重力场中通过涉及 4-6 个碱基对 (bp) 的弱杂交使固定在玻璃片上的微粒解离。当微粒上的声辐射力 (F) 和沉降力 (F) 的合力超过由于弱杂交而产生的结合力 (F) 时,微粒从玻璃片上解离。由于 F 和 F 可以通过微粒密度控制,并且 F 是施加到换能器的电压 (V) 的函数,因此增加 V 会诱导微粒解离。由于 20bp 的强杂交导致金纳米粒子 (AuNP) 结合到二氧化硅微粒 (SP) 上,SP 的密度增加,导致 F 和 F 增加; 因此,解离所需的电压 V 低于没有 AuNP 结合时所需的电压 V。我们证明了每个 SP 的 AuNP 结合数与 V 的依赖性符合理论预测。可以检测到 7500 个 AuNP 与 SP 之间的强杂交结合作为 V 的 10V 变化。本方法可以检测到涉及 AuNP 和 SP 之间强杂交的 2000 个 DNA 分子。

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