A sensitive electrochemical aptasensing platform based on exonuclease recycling amplification and host-guest recognition for detection of breast cancer biomarker HER2

被引:65
作者
Yang, Shuai [1 ]
You, Min [1 ]
Zhang, Fan [1 ]
Wang, Qingjiang [1 ]
He, Pingang [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200241, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical aptasensing; HER2; RecJ(f) exonuclease; Host-guest interaction; Homogeneous hybridization; ELECTRODE; APTAMER; CELLS; CHRONOCOULOMETRY; NANOPARTICLES; HYBRIDIZATION; IMMUNOSENSOR; OCHRATOXIN; BIOSENSOR; SERUM;
D O I
10.1016/j.snb.2017.11.119
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, a novel and sensitive electrochemical aptasensing platform was fabricated for the detection of the breast cancer biomarker HER2. HER2 aptamer was firstly hybridized with ferrocene-labeled DNA/Au nanospheres (FcNS), and then bound with the target HER2. The released FcNS homogeneously hybridized with horseradish peroxidase-labeled DNA/Au nanospheres (HRPNS). Benefiting from the introduction of RecJ(f) exonuclease, HER2 was recycled as the degradation of aptamer and bound another aptamer connected on FcNS. Thus, FcNS/HRPNS in large amounts was generated and captured by the modified Au electrode through the host-guest recognition between beta-cyclodextrin (beta-CD) and ferrocene (Fc). Horseradish peroxidase (HRP) catalyzed o-PD in presence of H2O2, producing a significantly amplified signal. Under the optimal conditions, the fabricated aptasensing platform showed an excellent sensitivity with a low detection limit of 4.9 ng ml(-1)(S/N = 3), and high specificity towards HER2. Furthermore, this proposed strategy presented the good reliability and applicability in the analysis of human serum samples, showing great potential for applications in early diagnosis of breast cancer. (c) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:796 / 802
页数:7
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