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An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay

Estrogen receptor (ER), expressed in approximately 80% of primary breast cancer cells, has proven to be a valuable predictive factor of the disease. Herein, by making use of the specific binding of ER to its DNA response elements, we propose an Exonuclease III (Exo III) protection-based electrochemi...

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Detalles Bibliográficos
Autores principales: Zhu, Sha, Cao, Ya, Xu, Yuanyuan, Yin, Yongmei, Li, Genxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3676839/
https://www.ncbi.nlm.nih.gov/pubmed/23681011
http://dx.doi.org/10.3390/ijms140510298
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author Zhu, Sha
Cao, Ya
Xu, Yuanyuan
Yin, Yongmei
Li, Genxi
author_facet Zhu, Sha
Cao, Ya
Xu, Yuanyuan
Yin, Yongmei
Li, Genxi
author_sort Zhu, Sha
collection PubMed
description Estrogen receptor (ER), expressed in approximately 80% of primary breast cancer cells, has proven to be a valuable predictive factor of the disease. Herein, by making use of the specific binding of ER to its DNA response elements, we propose an Exonuclease III (Exo III) protection-based electrochemical method for detecting ER proteins. In this assay, the presence of ER can protect the duplex DNA molecules immobilized on an electrode surface from Exo III-catalyzed digestion, resulting in an increased electrochemical signal. Experimental results have revealed that the proposed method can allow the quantification of ER in the range of 0.5 to 100 nM with a satisfactory detection limit of 0.38 nM. Furthermore, since this approach can also be employed to detect ER directly in nuclear extracts, it may be of great use in biomedical applications in the future.
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spelling pubmed-36768392013-07-02 An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay Zhu, Sha Cao, Ya Xu, Yuanyuan Yin, Yongmei Li, Genxi Int J Mol Sci Article Estrogen receptor (ER), expressed in approximately 80% of primary breast cancer cells, has proven to be a valuable predictive factor of the disease. Herein, by making use of the specific binding of ER to its DNA response elements, we propose an Exonuclease III (Exo III) protection-based electrochemical method for detecting ER proteins. In this assay, the presence of ER can protect the duplex DNA molecules immobilized on an electrode surface from Exo III-catalyzed digestion, resulting in an increased electrochemical signal. Experimental results have revealed that the proposed method can allow the quantification of ER in the range of 0.5 to 100 nM with a satisfactory detection limit of 0.38 nM. Furthermore, since this approach can also be employed to detect ER directly in nuclear extracts, it may be of great use in biomedical applications in the future. Molecular Diversity Preservation International (MDPI) 2013-05-16 /pmc/articles/PMC3676839/ /pubmed/23681011 http://dx.doi.org/10.3390/ijms140510298 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Zhu, Sha
Cao, Ya
Xu, Yuanyuan
Yin, Yongmei
Li, Genxi
An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay
title An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay
title_full An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay
title_fullStr An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay
title_full_unstemmed An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay
title_short An Exonuclease III Protection-Based Electrochemical Method for Estrogen Receptor Assay
title_sort exonuclease iii protection-based electrochemical method for estrogen receptor assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3676839/
https://www.ncbi.nlm.nih.gov/pubmed/23681011
http://dx.doi.org/10.3390/ijms140510298
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