放大器
化学
DNA
纳米技术
离子键合
生物传感器
信号(编程语言)
离子
聚合酶链反应
材料科学
基因
生物化学
有机化学
计算机科学
程序设计语言
作者
Xiaoqing Wu,Cheng Che,Xinmeng Wang,Qiujiao Du,Huageng Liang,Pengcheng Gao,Fan Xia
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2021-11-22
卷期号:93 (48): 16043-16050
被引量:21
标识
DOI:10.1021/acs.analchem.1c03631
摘要
DNA species are recognized as a powerful probe for nanochannel analyses to address the issues of specific target recognition and highly efficient signal conversion due to their programmable and predictable Watson–Crick bases. However, in the conventional view, abundant sophisticated DNA structures synthesized by DNA amplification strategies are unsuitable for use in nanochannel analyses owing to their low probability to enter a nanochannel restricted by the smaller opening of the nanochannel, as well as the faint ion signal produced by the steric effect. Here, we present an integrated strategy of nanochannel analyses that combines the target recognitions by encoded rolling circle amplification (RCA) in solution and the ionic signal enhancement by the space charge effect through the immobilization of highly negative-charged RCA amplicons on the outer surface of the nanochannels. Owing to the highly negative-charged RCA amplicons with 100 nm sizes, a sharp increase of ionic current up to 7454% has been achieved. The RCA amplicon triggered by mRNA-21 on the outer surface of the poly(ethylene terephthalate) membrane with a single nanochannel realized the single-base mismatch detection of mRNA-21 with a sensitivity of 6 fM. The DNA amplicon endows the nanochannel with high sensitivity and selectivity that could extend to other applications, such as DNA sequencing, desalination, sieving, and water–energy nexus.
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