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Novel colorimetric and fluorescent off-on enantiomers with high selectivity for Fe3+ imaging in living cells
被引:42
作者:
Fan, Chunhua
[1
]
Huang, Ximing
[1
]
Han, Liheng
[2
]
Lu, Zhengliang
[1
]
Wang, Zhuo
[3
]
Yi, Yuanping
[2
]
机构:
[1] Univ Jinan, Sch Chem & Chem Engn, Jinan 250022, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Key Lab Organ Solids, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[3] Beijing Univ Chem Technol, Fac Sci, Beijing 100029, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Chirality;
Fluorescent chemosensor;
Iron;
Living cell;
CIRCULARLY-POLARIZED LUMINESCENCE;
RHODAMINE-BASED FLUORESCENT;
IRON REGULATORY PROTEINS;
AQUEOUS-SOLUTION;
RATIONAL DESIGN;
CHEMOSENSOR;
SENSOR;
PROBE;
RECEPTOR;
POLYMER;
D O I:
10.1016/j.snb.2015.10.104
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Two novel colorimetric and fluorescent off-on enantiomers (R/S-RBOL) were developed to detect Fe3' in aqueous and biological samples through probing the integrated changes in fluorescence, circular dichroism (CD) and circularly polarized luminescence (CPL). The fluorescence intensity of R/S-RBOL is linearly proportional to the Fe3+ concentration in the range of 0-20 equiv., bringing out a detection limit of 1.83 x 10(-7)M. The Job's plot indicates a 1:1 binding stoichiometry of RBOL:Fe3+, which is further confirmed by ESI-MS analysis. Moreover, the RBOLs exhibit a dual-readout response in colour and fluorescence, rendering them suitable to sense Fe3+ in living cells with low cytotoxicity. In order to shed some light on the detection mechanism, the coordination between R/S-RBOL and Fe3+ is unravelled by DFT calculations. From the free RBOL to the RBOL-Fe3+ complex, the spiro-lactam ring is opened to interact with Fe3+ via the lactam N and O, imine N and hydroxyl 0 atoms in the form of a ferric six-coordinate structure. (C) 2015 Elsevier B.V. All rights reserved.
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页码:592 / 599
页数:8
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