Single-molecule porphyrin-metal ion interaction and sensing application

被引:29
作者
Wei, Keke [1 ]
Yao, Fujun [1 ]
Kang, Xiao-Feng [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Xian 710069, Shaanxi, Peoples R China
基金
美国国家科学基金会; 高等学校博士学科点专项科研基金;
关键词
alpha-hemolysin nanopore; Single-molecule detection; TPPS; Copper ion; Biosensor; ALPHA-HEMOLYSIN NANOPORE; COPPER IONS; PROTEIN NANOPORE; SELECTIVE DETECTION; BETA-CYCLODEXTRIN; CHEMICAL SENSOR; REAL-TIME; NANOPARTICLES; PORE; DNA;
D O I
10.1016/j.bios.2018.03.002
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
It remains a significant challenge to study the interactions between metal ions and porphyrin molecules at single ion level. Here, we constructed a nanopore-based sensing for label-free and real-time analysis of the interaction between Cu2+ and 5,10,15,20-tetrakis(4-sulfonatophenyl)-porphyrin (TPPS). The results demonstrate that emerging electronic signatures of the Cu2+-TPPS complex that is completely different form the original free TPPS were observed in the alpha-hemolysin (alpha-HL) nanopore. Based on the distinctive electronic signal patterns between TPPS and Cu2+-TPPS complex, the unique nanopore sensor can achieve a highly sensitive detection of Cu2+ in aqueous media. The frequency of signature events showed a linear response toward the concentration of Cu2+ in the range of 0.03 mu M - 1.0 mu M, with a detection limit of 16 nM (S/N = 3). The sensing system also exhibited high selectivity against other metal ions, and the feasibility of this approach for practical applications was demonstrated with the determination of Cu2+ in running water.
引用
收藏
页码:272 / 278
页数:7
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