4.7 Article

Highly sensitive electrochemical immunosensor for golgi protein 73 based on proximity ligation assay and enzyme-powered recycling amplification

期刊

ANALYTICA CHIMICA ACTA
卷 1040, 期 -, 页码 150-157

出版社

ELSEVIER
DOI: 10.1016/j.aca.2018.08.021

关键词

Golgi protein 73; Electrochemical immunosensor; Proximity ligation assay; Enzyme-powered recycling amplification

资金

  1. National Natural Science Foundation of China [21575025, 21575027]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT15R11]
  3. Program for Young Talents of Fujian Medical System [2015-ZQN-ZD-30]
  4. Social Development Guiding Programs of Fujian Province [2015Y0059]
  5. Science and Technology Program of Fujian Provincial Bureau of Quality and Technical Supervision [FJQI2014047]

向作者/读者索取更多资源

Golgi protein 73 (GP73) is a potential hepatocellular carcinoma serum marker with better sensitivity and specificity. In this study, a highly sensitive electrochemical immunosensor which combines the highly selective proximity ligation assay (PLA) and highly efficient enzyme-powered recycling amplification has been developed for GP73 determination. PLA is triggered by affinity binding of two labelled antibody-DNA (P1-RAb and P2-MAb) to target protein, resulting in increased specificity. The formed immunocomplex hybrids with DNA2 to realize the release of methylene blue labelled mononucleotides fragment with the help of exonuclease III, which acts as the power of recycling amplification. The fragment can diffuse easily to the nafion modified indium tin oxide electrode surface and a strong electrochemical signal can be detected. Under the optimized conditions, the enhanced electrochemical intensity has a linear relationship with the concentration of GP73 in the range of 0.3 pg mL(-1) to 6.0 ng mL(-1) with the detection limit of 0.10 pg mL(-1). The developed immunosensor has been applied to detect the GP73 in the clinical serum samples with satisfactory results. (C) 2018 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据