4.7 Article

Novel electrochemical nuclear factorkappa B biosensor via analyte-restrained peptide nucleic acid displacement reaction constructed on different gold nanoparticle-deposited carbon electrodes

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 335, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.129702

关键词

NF-kappa B biosensor; DNA binding protein; PNA/DNA displacement reaction; Gold nanoparticle-based signal amplification; Bovine mastitis

资金

  1. Natural Science Foundation of Jiangsu Province for Excellent Young Scholars [BK20170087]
  2. Fundamental Research Funds for the Central Universities [KYGD202001]
  3. Key Project of Inter-governmental International Scientific and Technological Innovation Cooperation [2018YFE0102200]
  4. Science and Technology Project of Xinjiang Production and Construction corps [2020AB025]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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This paper proposes an electrochemical biosensor for NF-κB based on a PNA displacement reaction, which is more suitable for detecting DNA binding proteins. The study shows that the portable SPCE has better analysis performance and is suitable for determining NF-κB in different samples. This sensor holds promising prospect in studying NF-κB-associated signal pathways and diagnosing inflammatory related diseases due to its commercialized mass production.
In this paper an electrochemical biosensor for NF-.B based on analyte-restrained peptide nucleic acid (PNA) displacement reaction is proposed, which is obviously more suitable for DNA binding proteins' detection compared with previous exonuclease cleavage methods. In our detection system, PNA probe is modified on gold nanoparticles (AuNPs) deposited carbon electrodes which could competitively conjugate with one strand of the designed dsDNA forming a PNA/DNA duplex. Methylene blue (MB), as electrochemical signal molecule, specifically inserts into PNA/DNA duplex significantly amplifying the electrochemical signal. When NF-kappa B is present in the detection system, it is able to be recognized and bound with dsDNA against PNA restraining the formation of PNA/DNA duplex, thus the electrochemical signal responding to the decrease of PNA/DNA duplex could be used to analyze the concentration of NF-kappa B. Then, detection performances based on two different carbon electrodes, glassy carbon electrode (GCE) and screen-printed carbon electrode (SPCE), are compared. The portable SPCE with a better analysis performance has a low detection limit at 2.7 pg mL(-1), which is more suitable for determining NF-kappa B in S. uberis-infected MECs sample. Benefit from commercialized mass production, it holds promising prospect in practical application in studying NF-kappa B-associated signal pathways and diagnosing inflammatory related diseases.

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