期刊
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 407, 期 9, 页码 2625-2630出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00216-015-8467-y
关键词
Chemical sensor; AIE fluorescent probe; Ag+ detection; cytosine-rich DNA; Enzyme
资金
- Natural Science Foundation of China [51373063, 21204027, 21221063]
- Research Fund for the Doctoral Program of Higher Education of China [20120061120016]
- Graduate Innovation Fund of Jilin University [2014082]
- [2013CB834702]
An aggregation-induced-emission (AIE)-active molecule, 4,4-(1E, 1E)-2,2-(anthracene-9,10-diyl) bis (ethene-2,1-diyl) bis (N,N,N-trimethylbenzenaminium iodide) (DSAI), used as a label-free and turn-on fluorescent probe, was developed for Ag+ sensing. The cytosine-rich DNA (oligo-C) chosen as a base could be induced to form a hairpin structure in the presence of Ag+. To improve the sensitivity of Ag+ detection, we selected nuclease S1 to reduce the fluorescence intensity of DSAI via its strong ability to hydrolyze oligo-C. In the solution containing oligo-C, DSAI, and nuclease S1, in the absence of Ag+, oligo-C was broken into fragments by nuclease S1; this meant DSAI could not aggregate, leading to non-emission of the solution. In the presence of Ag+, oligo-C was induced to form a hairpin structure via the C-Ag+-C base pair and DSAI could aggregate on the surface of the hairpin structure to produce a strong emission. On increasing the amount of Ag+ in the solution containing oligo-C, DSAI, and nuclease S1, the fluorescence intensity of DSAI gradually increased, and the highest intensity was nearly 16-fold higher than the original intensity. The detection limit at a signal-to-noise ratio (S/N) of 3 was estimated to be 155 nmol L-1. The new sensing method provides simplicity, easy operation, and good sensitivity and selectivity for Ag+ detection.
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