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基于 DNA 链置换的快速可视化验证。

Rapid Visual Authentication Based on DNA Strand Displacement.

机构信息

US Army Combat Capabilities Development Command Chemical Biological Center, Aberdeen Proving Ground, Edgewood, Maryland 21010, United States.

Applied DNA Sciences, Stony Brook, New York 11790, United States.

出版信息

ACS Appl Mater Interfaces. 2021 Apr 28;13(16):19476-19486. doi: 10.1021/acsami.1c02429. Epub 2021 Apr 14.

Abstract

Novel ways to track and verify items of a high value or security is an ever-present need. Taggants made from deoxyribonucleic acid (DNA) have several advantageous properties, such as high information density and robust synthesis; however, existing methods require laboratory techniques to verify, limiting applications. Here, we leverage DNA nanotechnology to create DNA taggants that can be validated in the field in seconds to minutes with a simple equipment. The system is driven by toehold-mediated strand-displacement reactions where matching oligonucleotide sequences drive the generation of a fluorescent signal through the potential energy of base pairing. By pooling different "input" oligonucleotide sequences in a taggant and spatially separating "reporter" oligonucleotide sequences on a paper ticket, unique, sequence-driven patterns emerge for different taggant formulations. Algorithmically generated oligonucleotide sequences show no crosstalk and ink-embedded taggants maintain activity for at least 99 days at 60 °C (equivalent to nearly 2 years at room temperature). The resulting fluorescent signals can be analyzed by the eye or a smartphone when paired with a UV flashlight and filtered glasses.

摘要

追踪和验证高价值或高安全性物品的新方法是一个永恒的需求。由脱氧核糖核酸 (DNA) 制成的标记物具有几个优势特性,例如高信息密度和稳健的合成;然而,现有的方法需要实验室技术来验证,限制了其应用。在这里,我们利用 DNA 纳米技术来创建 DNA 标记物,可以在几秒钟到几分钟内用简单的设备在现场进行验证。该系统由链置换反应驱动,其中匹配的寡核苷酸序列通过碱基配对的势能驱动荧光信号的产生。通过在标记物中汇集不同的“输入”寡核苷酸序列,并在纸质票证上空间分离“报告”寡核苷酸序列,不同标记物配方会出现独特的、序列驱动的模式。算法生成的寡核苷酸序列没有串扰,并且嵌入油墨的标记物在 60°C 下至少保持 99 天的活性(相当于室温下近 2 年)。当与紫外线手电筒和滤光眼镜配合使用时,产生的荧光信号可以用肉眼或智能手机进行分析。

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