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Nitrogen-doped graphene quantum dots-labeled epitope imprinted polymer with double templates via the metal chelation for specific recognition of cytochrome c
被引:66
作者:
Yan, Yun-Jing
[1
]
He, Xi-Wen
[1
]
Li, Wen-You
[1
,2
]
Zhang, Yu-Kui
[1
,3
]
机构:
[1] Nankai Univ, State Key Lab Med Chem Biol, Tianjin Key Lab Biosensing & Mol Recognit, Coll Chem,Res Ctr Analyt Sci, Tianjin 300071, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
[3] Chinese Acad Sci, Natl Chromatog Res & Anal Ctr, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Surface imprinting;
Nitrogen-doped graphene quantum dots;
Epitope imprinting;
Metal chelation;
Fluorescent sensor;
ONE-POT SYNTHESIS;
FLUORESCENCE DETECTION;
SURFACE;
NANOPARTICLES;
PROTEIN;
PEPTIDES;
QUANTIFICATION;
GROWTH;
BEADS;
D O I:
10.1016/j.bios.2016.12.040
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
A novel fluorescent sensor nitrogen-doped graphene quantum dots (N-GQDs)/SiO2/molecular imprinting polymer ( N-GQDs/SiO2/MIP) was fabricated by surface imprinting and epitope imprinting to recognize and detect the target protein cytochrome c (Cyt C) with fluorescence quenching. In the polymerization process, the C- and N-terminal nonapeptides of Cyt C were selected as the double templates which were fixed by functional monomer (zinc acrylate) through metal chelation and steady six-membered ring. The linear range of fluorescence quenching for this receptor towards Cyt C was 0.20-60 mu M, and the detection limit was 0.11 mu M. The precision for six times replicate determination of Cyt C at 30 M was 1.20%, and the imprinting factor (IF) was 3.06. The recoveries of the material to Cyt C in urine were 99.3-114.0%. In brief, this work proposed a strategy to prepare a new type fluorescent imprinting polymer based on N-GQDs and provided an attractive perspective for the detection of protein by using the combination of N-GQDs and molecular imprinting technique.
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页码:253 / 261
页数:9
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