化学
检出限
生物传感器
核酸外切酶 III
纳米技术
纳米颗粒
自组装
微流控
DNA
滚动圆复制
色谱法
材料科学
有机化学
基因
DNA复制
生物化学
大肠杆菌
作者
Caijun Wu,Siqi Huang,Yuying Wang,Yaqin Chai,Ruo Yuan,Xia Yang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2021-07-29
卷期号:93 (31): 11019-11024
被引量:41
标识
DOI:10.1021/acs.analchem.1c02336
摘要
Au nanoparticles (Au NPs) can be self-assembled in a bottom-up orderly manner at the oil–water interface, which is widely used as SERS platforms, but the stability of the Au NP interface needs to be improved due to shaking or shifting and the Brownian motion. The DNA structure with unique sequence specificity, excellent programmability, and flexible end-group modification capability owns good potential to precisely control the plasmonic structure's distance. In this study, a large area of the SERS substrate is obtained from the DNA structure-stabilized self-assembled ordered Au NPs on the cyclohexane–water interface. Combining with the exonuclease III (exo III)-assisted DNA recycling amplification strategy, we construct a liquid-phase SERS biosensor for efficient detection of microRNA 155 (miRNA 155). Compared with the traditional randomly assembled Au NPs on the two-phase interface, the SERS signal is significantly enhanced and more stable. The detection limit of the SERS biosensor for miRNA 155 reached 1.45 fmol/L, which has a very wide linear range (100 fmol/L–5 nmol/L). This work gives an efficient approach to stabilize the self-assembly Au NPs on the liquid–liquid interface, which can broaden the application of SERS analysis.
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