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基于含有G-四链体结构域的茎环探针的无标记逻辑模块和两层级联。

Label-free logic modules and two-layer cascade based on stem-loop probes containing a G-quadruplex domain.

作者信息

Guo Yahui, Cheng Junjie, Wang Jine, Zhou Xiaodong, Hu Jiming, Pei Renjun

机构信息

Suzhou Key Laboratory of Nanotheranostics, Division of Nanobiomedicine, Collaborative Innovation Center of Suzhou Nano Science and Technology, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, 215123 (P.R. China); Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry & Molecular Sciences, Wuhan University, Wuhan, 430072 (P.R. China).

出版信息

Chem Asian J. 2014 Sep;9(9):2397-401. doi: 10.1002/asia.201402199. Epub 2014 Jun 6.

Abstract

A simple, versatile, and label-free DNA computing strategy was designed by using toehold-mediated strand displacement and stem-loop probes. A full set of logic gates (YES, NOT, OR, NAND, AND, INHIBIT, NOR, XOR, XNOR) and a two-layer logic cascade were constructed. The probes contain a G-quadruplex domain, which was blocked or unfolded through inputs initiating strand displacement and the obviously distinguishable light-up fluorescent signal of G-quadruplex/NMM complex was used as the output readout. The inputs are the disease-specific nucleotide sequences with potential for clinic diagnosis. The developed versatile computing system based on our label-free and modular strategy might be adapted in multi-target diagnosis through DNA hybridization and aptamer-target interaction.

摘要

通过使用引发链置换的toehold和茎环探针,设计了一种简单、通用且无标记的DNA计算策略。构建了全套逻辑门(是、非、或、与非、与、抑制、或非、异或、同或)和一个两层逻辑级联。这些探针包含一个G-四链体结构域,该结构域通过引发链置换的输入被阻断或展开,并且G-四链体/NMM复合物明显可区分的点亮荧光信号被用作输出读数。输入是具有临床诊断潜力的疾病特异性核苷酸序列。基于我们无标记且模块化策略开发的通用计算系统可能适用于通过DNA杂交和适体-靶标相互作用进行多靶点诊断。

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