An electrochemical biosensor for the assay of alpha-fetoprotein-L3 with practical applications

被引:60
作者
Li, Jinlong [1 ,2 ,3 ]
Gao, Tao [1 ,2 ]
Gu, Shiyu [1 ,2 ]
Zhi, Jun [1 ,2 ]
Yang, Jie [1 ,2 ]
Li, Genxi [1 ,2 ,4 ]
机构
[1] Nanjing Univ, Dept Biochem, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Dept Biochem, Collaborat Innovat Ctr Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[3] Southeast Univ, Affiliated Hosp 2, Dept Lab Med, Nanjing 210003, Peoples R China
[4] Shanghai Univ, Sch Life Sci, Ctr Mol Recognit & Biosensing, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical biosensor; AFP-L3; Lens culinaris agglutinin; GOLGI PROTEIN 73; ALPHA-FETOPROTEIN; HEPATOCELLULAR-CARCINOMA; SIGNAL AMPLIFICATION; GRAPHENE; SURFACE; DNA; NANOPARTICLES; IMMUNOSENSOR; IMMUNOASSAY;
D O I
10.1016/j.bios.2016.08.071
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The detection of alpha-fetoprotein-L3 (AFP-L3) is of great importance for hepatocellular carcinoma (HCC) diagnosis, but remains unsatisfactory owing to poor sensitivity and complex operating steps. In this work, a simple and sensitive method has been proposed for the detection of AFP-L3. Firstly, biotinylated Lens culinaris agglutinin-integrated silver nanoparticles (B-LCA-AgNPs) is fabricated. Owing to the specific interaction between Lens culinaris agglutinin and AFP-L3, AFP-L3 can be detected directly through the electrochemical signal readout of AgNPs, avoiding separated steps used in clinical practice. Furthermore, after the recognition between B-LCA-AgNPs and AFP-L3, large amount of AgNPs can be gathered at the binding site through avidin-biotin interactions, which can amplify the signal. Therefore, detection of AFP-L3 can be sensitively achieved. Moreover, compared with the other approaches, this new method has a better linear correlation (25-15,000 pg/mL) and a lower detection limit (12 pg/mL). Also, the new method developed in this work has been demonstrated to have good stability and reproducibility for the assay of AFP-L3 in human serum samples, so, it may hold a great application prospect in clinical diagnostics. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:352 / 357
页数:6
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