文献类型：期刊文献

英文题名：A Selective Surface-Enhanced Raman Scattering Sensor for Mercury(II) Based on a Porous Polymer Material and the Target-Mediated Displacement of a T-Rich Strand

作者：Kang, Y.;Zhang, L.;Zhang, H.;Wu, T.;Du, Y.[1]

机构：[1]East China Univ Sci & Technol, Sch Chem & Mol Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China; East China Univ Sci & Technol, Res Ctr Anal & Test, 130 Meilong Rd, Shanghai 200237, Peoples R China

年份：2017

卷号：84

期号：2

起止页码：225

外文期刊名：JOURNAL OF APPLIED SPECTROSCOPY

收录：;EI(收录号：20242616439961);WOS:【SCI-EXPANDED(收录号:WOS:000405099700004)】；

基金：We are thankful to the Special Funded Projects of the Fundamental Research Funds from the Chinese Academy of Inspection and Quarantine of China (Grant No. 2013JK017). The authors are grateful to Dr L. F. Zhang, X. Wang, and L. Zhang for helpful discussions.

语种：英文

外文关键词：mercury ion; surface-enhanced Raman scattering; aptamer; T-Hg2+-T; glycidyl methacrylate-ethylene dimethacrylate material

摘要：A sensitive and selective surface-enhanced Raman scattering (SERS) sensor for mercury(II) was fabricated based on the target-mediated displacement of a T-rich oligonucleotide strand. A DNA/aptamer duplex was prepared by the hybridization between a tetramethylrhodamine(TMR)-labeled thymine(T)-rich Hg2+-specific aptamer (denoted as TMR-aptamer) and a thiolated adenine-rich capturing DNA. The duplex can be immobilized onto the SERS substrate of the Ag-moiety modified glycidyl methacrylate-ethylene dimethacrylate (denoted as Ag-GMA-EDMA) via self-assembly by the thiol anchor, in which the TMR-aptamer exists in a double-stranded chain. In this case, the label of the TMR moiety approaches the substrate surface and produces a strong SERS signal. Upon the addition of the target, a pair of TMR-aptamers could cooperatively coordinate with Hg2+ to form a stable duplex-like structure mediated by the T-Hg2+-T complex between two adjacent strands, which triggers the release of the TMR-aptamer from the SERS substrate surface, thus drawing the TMR tags away from the substrate with a significant decrease in the SERS signal. This optical sensor shows a sensitive response to Hg2+ in a concentration from 5 nM to 2.0 mu M with a detection limit of 2.5 nM. The prepared sensor is negligibly responsive to other metal ions, can be easily regenerated, and shows good performance in real sample analysis.