An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach

Protein is a kind of basic substance that constitutes a life body. The determination of protein is very important for the research of biology, medicine, and other fields. Lysozyme is relatively small and simple in structure among all kinds of proteins, so it is often used as a standard target detect...

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Autores principales: Song Kai, Chen Wenwu
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Lenguaje:EN
Publicado: De Gruyter 2021
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Acceso en línea:https://doaj.org/article/019a673157464e3ba2f9c9c7f57e80f1
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spelling oai:doaj.org-article:019a673157464e3ba2f9c9c7f57e80f12021-12-05T14:10:43ZAn electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach2391-542010.1515/chem-2021-0026https://doaj.org/article/019a673157464e3ba2f9c9c7f57e80f12021-03-01T00:00:00Zhttps://doi.org/10.1515/chem-2021-0026https://doaj.org/toc/2391-5420Protein is a kind of basic substance that constitutes a life body. The determination of protein is very important for the research of biology, medicine, and other fields. Lysozyme is relatively small and simple in structure among all kinds of proteins, so it is often used as a standard target detector in the study of aptamer sensor for protein detection. In this paper, a lysozyme electrochemical sensor based on aptamer competition mechanism is proposed. We have successfully prepared a signal weakening electrochemical sensor based on the lysozyme aptamer competition mechanism. The carboxylated multi-walled carbon nanotubes (MWCNTs) were modified on the glassy carbon electrode, and the complementary aptamer DNA with amino group was connected to MWCNTs. Because of the complementary DNA of daunomycin into the electrode, the electrochemical signal is generated. When there is a target, the aptamer binds to lysozyme with higher binding power, and the original complementary chain breaks down, resulting in the loss of daunomycin inserted into the double chain and the weakening of electrochemical signal. Differential pulse voltammetry was used to determine lysozyme, the response range was 1–500 nM, the correlation coefficient was 0.9995, and the detection limit was 0.5 nM. In addition, the proposed sensor has good selectivity and anti-interference.Song KaiChen WenwuDe Gruyterarticledifferential pulse voltammetrylysozymedaunomycinaptamermulti-walled carbon nanotubeselectrochemical analysisChemistryQD1-999ENOpen Chemistry, Vol 19, Iss 1, Pp 299-306 (2021)
institution DOAJ
collection DOAJ
language EN
topic differential pulse voltammetry
lysozyme
daunomycin
aptamer
multi-walled carbon nanotubes
electrochemical analysis
Chemistry
QD1-999
spellingShingle differential pulse voltammetry
lysozyme
daunomycin
aptamer
multi-walled carbon nanotubes
electrochemical analysis
Chemistry
QD1-999
Song Kai
Chen Wenwu
An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
description Protein is a kind of basic substance that constitutes a life body. The determination of protein is very important for the research of biology, medicine, and other fields. Lysozyme is relatively small and simple in structure among all kinds of proteins, so it is often used as a standard target detector in the study of aptamer sensor for protein detection. In this paper, a lysozyme electrochemical sensor based on aptamer competition mechanism is proposed. We have successfully prepared a signal weakening electrochemical sensor based on the lysozyme aptamer competition mechanism. The carboxylated multi-walled carbon nanotubes (MWCNTs) were modified on the glassy carbon electrode, and the complementary aptamer DNA with amino group was connected to MWCNTs. Because of the complementary DNA of daunomycin into the electrode, the electrochemical signal is generated. When there is a target, the aptamer binds to lysozyme with higher binding power, and the original complementary chain breaks down, resulting in the loss of daunomycin inserted into the double chain and the weakening of electrochemical signal. Differential pulse voltammetry was used to determine lysozyme, the response range was 1–500 nM, the correlation coefficient was 0.9995, and the detection limit was 0.5 nM. In addition, the proposed sensor has good selectivity and anti-interference.
format article
author Song Kai
Chen Wenwu
author_facet Song Kai
Chen Wenwu
author_sort Song Kai
title An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
title_short An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
title_full An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
title_fullStr An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
title_full_unstemmed An electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
title_sort electrochemical sensor for high sensitive determination of lysozyme based on the aptamer competition approach
publisher De Gruyter
publishDate 2021
url https://doaj.org/article/019a673157464e3ba2f9c9c7f57e80f1
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AT chenwenwu anelectrochemicalsensorforhighsensitivedeterminationoflysozymebasedontheaptamercompetitionapproach
AT songkai electrochemicalsensorforhighsensitivedeterminationoflysozymebasedontheaptamercompetitionapproach
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