Pu Wendan, Zhao Zhao, Wu Liping, Liu Yue, Zhao Huawen
J Nanosci Nanotechnol. 2015 Aug;15(8):5524-9. doi: 10.1166/jnn.2015.10293.
A sensitive label-free method was presented for the determination of silver ion (Ag+) in this paper. Cytosine-rich DNA (C-DNA) was used as Ag+ specific DNA. Without Ag+ in the solution, fluorescence of fluorescein (FAM) is quenched by C-DNA stabilized gold nanoparticles (AuNPs) in high salt environment. When Ag+ is present in the solution, however, Ag+-mediated cytosine-Ag+-cytosine (C-Ag+-C) base pairs induced the C-DNA folding into a hairpin structure, which can not stabilize AuNPs in high salt environment, thus causing AuNPs aggregation. After centrifugation to remove the aggregated AuNPs, the quenching ability of the supernatant for FAM is decreased and the fluorescence intensity of solution increases with increasing the Ag+ concentration. Due to the highly specific interaction of the C-DNA towards Ag+ and the strong fluorescent quenching ability of AuNPs for FAM, the method has high selectivity and sensitivity for Ag+. Under the optimal conditions, the fluorescence intensity at 515 nm increased linearly with the concentration of Ag+ ranging from 15 nM to 700 nM, and the detection limit was determined as 6 nM based on 3 σ/slope. This method is simple, sensitive, and may be applied to other detection systems by selecting the appropriate DNA sequences.
本文提出了一种灵敏的无标记方法用于测定银离子(Ag+)。富含胞嘧啶的DNA(C-DNA)被用作Ag+特异性DNA。在溶液中没有Ag+时,在高盐环境下,荧光素(FAM)的荧光被C-DNA稳定的金纳米颗粒(AuNPs)淬灭。然而,当溶液中存在Ag+时,Ag+介导的胞嘧啶-Ag+-胞嘧啶(C-Ag+-C)碱基对会诱导C-DNA折叠成发夹结构,在高盐环境下该结构无法稳定AuNPs,从而导致AuNPs聚集。离心去除聚集的AuNPs后,上清液对FAM的淬灭能力降低,溶液的荧光强度随Ag+浓度的增加而增加。由于C-DNA与Ag+之间具有高度特异性相互作用以及AuNPs对FAM具有较强的荧光淬灭能力,该方法对Ag+具有高选择性和高灵敏度。在最佳条件下,515 nm处的荧光强度随Ag+浓度在15 nM至700 nM范围内呈线性增加,基于3σ/斜率确定检测限为6 nM。该方法简单、灵敏,通过选择合适的DNA序列可应用于其他检测系统。