Facile electrochemical biosensor based on a new bifunctional probe for label-free detection of CGG trinucleotide repeat

被引:25
作者
He, Hanping [1 ]
Xia, Jingping [1 ]
Peng, Xiaoqian [1 ]
Chang, Gang [2 ]
Zhang, Xiuhua [1 ]
Wang, Yafen [1 ]
Nakatani, Kazuhiko [3 ]
Lou, Zhaowen [1 ]
Wang, Shengfu [1 ]
机构
[1] Hubei Univ, Coll Chem & Chem Engineer, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Minist Educ,Key Lab Synth & Applicat Organ Funct, Wuhan 430062, Hubei, Peoples R China
[2] Hubei Univ, Coll Mat Sci & Engn, Minist Educ, Key Lab Green Preparat & Applicat Funct Mat, Wuhan 430062, Hubei, Peoples R China
[3] Osaka Univ, ISIR, Dept Regulatory Bioorgan Chem, Ibaraki 5670047, Japan
基金
中国国家自然科学基金; 湖北省教育厅重点项目;
关键词
Electrochemical biosensor; Trinucleotide repeat; Recognition of CGG; Ferrocenyl modified naphthyridine derivative; GENETIC INSTABILITY; METHYLENE-BLUE; DNA; SURFACES; BINDING; GOLD;
D O I
10.1016/j.bios.2013.05.022
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We have developed a simple and label-free electrochemical assay to detect CGG trinucleotide repeat. For this purpose, a new bifunctional probe (FecNCD2) was developed, in which a recognition part (naphthyridine carbamate dimmer, NCD) was connected with an electro-active part (ferrocenyl group) using a chain of -CO-NH-CH2-CH2-. The results of circular dichroismic measurements indicated that FecNCD2 exhibited a superior performance for selective binding to CGG trinucleotide repeats compared to a previous bifunctional electrochemical probe connected with shorter linker -CH2- (FecNCD1). Then, the electrochemical properties of FecNCD2 were evaluated and were found to show a good redox response due to the ferrocene moiety. Owing to the high performances of FecNCD2, the label-free electrochemical biosensor for CGG repeats was constructed by immobilizing them onto gold disk electrode and by using FecNCD2 as an electrochemical probe in solution. Further CGG repeats in solution were confirmed to be detectable using the CGG modified biosensor in competitive experiments, i.e., by treating it in test solutions containing FecNCD2 and d(CGG)(10) or others. No interference of ct-DNA on the CGG detection was also confirmed with this approach. The strategy should have significant potential for the development of versatile and low-cost biosensor for early diagnosis and treatment of neurodegenerative diseases associated with trinucleotide repeats. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:282 / 289
页数:8
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