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.
引用
收藏
页码:253 / 261
页数:9
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