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A Highly Sensitive and Selective Competition Assay for the Detection of Cysteine Using Mercury-Specific DNA, Hg2+ and Sybr Green I
被引:13
作者:
Xu, Hui
[1
]
Gao, Shuli
[1
]
Liu, Quanwen
[1
]
Pan, Dun
[2
]
Wang, Lihua
[2
]
Ren, Shuzhen
[3
]
Ding, Min
[3
]
Chen, Jingwen
[3
]
Liu, Gang
[3
]
机构:
[1] Ludong Univ, Sch Chem & Mat Sci, Yantai 264025, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Phys Biol Lab, Shanghai 201800, Peoples R China
[3] Shanghai Inst Measurement & Testing Technol, Shanghai 201203, Peoples R China
来源:
关键词:
cysteine;
competition assay;
mercury-specific DNA;
Hg2+;
Sybr Green I;
PERFORMANCE LIQUID-CHROMATOGRAPHY;
FLOW-INJECTION DETERMINATION;
CARBON-PASTE ELECTRODE;
GOLD NANOPARTICLES;
N-ACETYLCYSTEINE;
METAL-COMPLEXES;
ASCORBIC-ACID;
AMINO-ACIDS;
GLUTATHIONE;
CONSTANTS;
D O I:
10.3390/s111110187
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
We here report a rapid, sensitive, selective and label-free fluorescence detection method for cysteine (Cys). The conformation of mercury-specific DNA (MSD) changes from a random coil form to a hairpin structure in the presence of Hg2+ due to the formation of a thymine-Hg2+-thymine (T-Hg2+-T) complex. Cys can selectively coordinate with Hg2+ and extract it from the thymine-Hg2+-thymine complex. The hairpin structure dehybridizes and the fluorescence intensity of Sybr Green I (SG) decreases upon addition of Cys because SG efficiently discriminates mercury-specific DNA and mercury-specific DNA/Hg2+ complex. The detection can be finished within 5 min with high sensitivity and selectivity. In addition, we can obtain variable dynamic ranges for Cys by changing the concentration of MSD/Hg2+.
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页码:10187 / 10196
页数:10
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