共 41 条
A fluorometric histidine biosensor based on the use of a quencher-labeled Cu(II)-dependent DNAzyme
被引:19
作者:
Chen, Zhuling
[1
]
He, Qun
[2
]
Zhao, Mengmeng
[3
]
Lin, Cuiying
[1
]
Luo, Fang
[3
,4
]
Lin, Zhenyu
[3
]
Chen, Guonan
[3
]
机构:
[1] Fuzhou Univ, Coll Chem, Fuzhou 350116, Fujian, Peoples R China
[2] Fuzhou Univ, Sch Law, Fuzhou 350116, Fujian, Peoples R China
[3] Fuzhou Univ, Fujian Prov Key Lab Anal & Detect Food Safety, Minist Educ, Key Lab Anal & Detect Food Safety, Fuzhou 350116, Fujian, Peoples R China
[4] Fuzhou Univ, Coll Biol Sci & Engn, Fuzhou 350116, Fujian, Peoples R China
关键词:
DNAzyme;
Cofactors;
FAM-labeled DNA;
Catalytic beacon;
Fluorometry;
Human urine samples;
AMINO-ACIDS;
AMPLIFIED DETECTION;
FLUORESCENT-PROBE;
DNA;
ELECTROPHORESIS;
OXIDATION;
ENSEMBLE;
CLEAVAGE;
PLASMA;
D O I:
10.1007/s00604-017-2425-7
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
The authors describe a biosensor for histidine that is based on the use of a DNAzyme catalytic beacon. The Cu(II)-dependent DNA-cleaving DNAzyme (Cu-Enzyme) was modified with a quencher (BHQ1) at its 5' end, and the corresponding substrate strand (Cu-Sub) was modified with a quencher and the FAM fluorophore at its 5' and 3' ends, respectively. The green FAM emission of the system is completely quenched after the Cu-Enzyme is hybridized with Cu-Sub. The presence of Cu(II) triggers the cleavage of the Cu-Sub so that fluorescence recovers. Histidine forms a complex with Cu(II) ion. The complex is not capable of cleaving Cu-Sub effectively so that the fluorescence of the system is not restored. These findings were exploited to design a robust and sensitive assay for the determination of histidine. Fluorescence intensity is linearly related to the concentration of histidine in the range between 0.05 and 40 mu M, and the detection limit is 20 nM. The method has been successfully applied to the determination of histidine in (spiked) human urine and gave satisfying results.
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页码:4015 / 4020
页数:6
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