Molecular switch-modulated fluorescent copper nanoclusters for selective and sensitive detection of histidine and cysteine

被引:23
作者
Gu, Zefeng [1 ]
Cao, Zhijuan [1 ]
机构
[1] Fudan Univ, Sch Pharm, 826 Zhangheng Rd, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
Dumbbell DNA template; Histidine; Cysteine; Logic gate; Fluorescent copper nanoclusters; TURN-ON DETECTION; QUANTUM DOTS; HUMAN URINE; GOLD NANOPARTICLES; METAL NANOCLUSTERS; PROBE; ENSEMBLE; HOMOCYSTEINE; SYSTEM; BIOTHIOLS;
D O I
10.1007/s00216-018-1149-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel assay for histidine and cysteine has been constructed based on modulation of fluorescent copper nanoclusters (CuNCs) by molecular switches. In our previous work, a dumbbell DNA template with a poly-T (thymine) loop has been developed as an excellent template for the formation of strongly fluorescent CuNCs. Herein, for the first time, we established this biosensor for sensing two amino acids by using dumbbell DNA-templated CuNCs as the single probe. Among 20 natural amino acids, only histidine and cysteine can selectively quench fluorescence emission of CuNCs, because of the specific interaction of these compounds with copper ions. Furthermore, by using nickel ions (Ni2+) and N-ethylmaleimide as the masking agents for histidine and cysteine respectively, an integrated logic gate system was designed by coupling with the fluorescent CuNCs and demonstrated selective and sensitive detection of cysteine and histidine. Under optimal conditions, cysteine can be detected in the concentration ranges of 0.01-10.0 mu M with the detection limit (DL) of as low as 98 pM, while histidine can be detected in the ranges of 0.05-40.0 mu M with DL of 1.6 nM. In addition, histidine and cysteine can be observed with the naked eye under a hand-held UV lamp (DL, 50 nM), which can be easily adapted to automated high-throughput screening. Finally, the strategy has been successfully utilized for biological fluids. The proposed system can be conducted in homogeneous solution, eliminating the need for organic cosolvents, separation processes of nanomaterials, or any chemical modifications. Overall, the assay provides an alternative method for simultaneous detection of cysteine and histidine by taking the advantages of high speed, no label and enzyme requirement, and good sensitivity and specificity, and will satisfy the great demand for determination of amino acids in fields such as food processing, biochemistry, pharmaceuticals, and clinical analysis.
引用
收藏
页码:4991 / 4999
页数:9
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