适体
荧光
检出限
核酸外切酶 III
化学
核酸外切酶
胞嘧啶
选择性
线性范围
离子
分析化学(期刊)
组合化学
光化学
色谱法
DNA
生物化学
分子生物学
有机化学
生物
大肠杆菌
物理
基因
DNA聚合酶
催化作用
量子力学
作者
Zhiwen Wei,Yi‐Feng Lan,Chao Zhang,Juan Jia,Weifen Niu,Yanli Wei,Shanlin Fu,Keming Yun
标识
DOI:10.1016/j.saa.2021.119927
摘要
Based on the specific interaction of Ag+ and cytosine-cytosine (C-C) base mismatch and using berberine (Ber) as the fluorescent probe and Exonuclease I (Exo I) as the background fluorescence reducing tool, a label-free Exo I-assisted fluorescence aptamer sensing platform was established for the detection of silver ions with high sensitivity and selectivity. Exo I reduced the fluorescence background of the Ber/Ag+-aptamer complex to a level similar to that of Ber itself in the absence of Ag+. After introducing Ag+ into the sensing system, it induces the aptamer rich in base C to form C-Ag+-C i-motif structure which are resistant to degradation mediated by Exo I. The concentration of Ber, Ag+-aptamer, Exo I and the temperature and reaction time for Exo I were all optimized. Under the optimal experimental conditions, the detection limit of Ag+ was 4.4 nM and the linear range was from 0.0059 μM to 235.48 μM with a coefficient of determination (R2) > 0.99. Moreover, the proposed strategy had been successfully applied to the detection of Ag+ in tap water and human serum with a good recovery ranging from 88.4% to 106.9%.
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