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用于生物传感的变增益 DNA 纳米结构电荷放大器。

Variable gain DNA nanostructure charge amplifiers for biosensing.

机构信息

Microsystems and Nanotechnology Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

Biomolecular Measurement Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

出版信息

Nanoscale. 2024 Nov 21;16(45):20893-20902. doi: 10.1039/d4nr02959c.

Abstract

Electronic measurements of engineered nanostructures comprised solely of DNA (DNA origami) enable new signal conditioning modalities for use in biosensing. DNA origami, designed to take on arbitrary shapes and allow programmable motion triggered by conjugated biomolecules, have sufficient mass and charge to generate a large electrochemical signal. Here, we demonstrate the ability to electrostatically control the DNA origami conformation, and thereby the resulting signal amplification, when the structure binds a nucleic acid analyte. Critically, unlike previous studies that employ DNA origami to amplify an electrical signal, we show that the conformation changes under an applied field are reversible. This applied field also simultaneously accelerates structural transitions above the rate determined by thermal motion. We tuned this property of the structures to achieve a response that was ≈2 × 10 times greater (, a gain or amplification) than the value from DNA hybridization under similar conditions. Because this signal amplification is independent of DNA origami-analyte interactions, our approach is agnostic of the end application. Furthermore, since large signal changes are only triggered in response to desirable interactions, we minimize the deleterious effects of non-specific binding. The above benefits of self-assembled DNA origami make them ideally suited for multiplexed biosensing when paired with highly parallel electronic readout.

摘要

电子测量工程 DNA(折纸 DNA)纳米结构仅启用新的信号调理方式用于生物传感。DNA 折纸,旨在采取任意形状,并允许共轭生物分子触发可编程运动,具有足够的质量和电荷,以产生大的电化学信号。在这里,我们展示了在结构结合核酸分析物时,静电控制 DNA 折纸构象的能力,从而实现了信号放大。至关重要的是,与以前采用 DNA 折纸放大电信号的研究不同,我们表明在施加电场下的构象变化是可逆的。该外加电场还同时加速了结构转变,使其超过由热运动决定的速率。我们调整了结构的这种特性,以实现比类似条件下 DNA 杂交产生的响应高约 20 倍的响应(增益或放大)。由于这种信号放大与 DNA 折纸-分析物相互作用无关,因此我们的方法不受最终应用的限制。此外,由于仅在响应期望相互作用时才触发大的信号变化,因此我们将非特异性结合的有害影响降至最低。自组装 DNA 折纸的上述优点使其非常适合与高度并行的电子读出配对进行多重生物传感。

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本文引用的文献

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