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A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1
Human arylamine N-acetyltransferase 1 (hNAT1) has become an attractive potential biomarker for estrogen-receptor-positive breast cancers. We describe here the mechanism of action of a selective non-covalent colorimetric biosensor for the recognition of hNAT1 and its murine homologue, mNat2, over the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734253/ https://www.ncbi.nlm.nih.gov/pubmed/23940600 http://dx.doi.org/10.1371/journal.pone.0070600 |
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author | Laurieri, Nicola Egleton, James E. Varney, Amy Thinnes, Cyrille C. Quevedo, Camilo E. Seden, Peter T. Thompson, Sam Rodrigues-Lima, Fernando Dairou, Julien Dupret, Jean-Marie Russell, Angela J. Sim, Edith |
author_facet | Laurieri, Nicola Egleton, James E. Varney, Amy Thinnes, Cyrille C. Quevedo, Camilo E. Seden, Peter T. Thompson, Sam Rodrigues-Lima, Fernando Dairou, Julien Dupret, Jean-Marie Russell, Angela J. Sim, Edith |
author_sort | Laurieri, Nicola |
collection | PubMed |
description | Human arylamine N-acetyltransferase 1 (hNAT1) has become an attractive potential biomarker for estrogen-receptor-positive breast cancers. We describe here the mechanism of action of a selective non-covalent colorimetric biosensor for the recognition of hNAT1 and its murine homologue, mNat2, over their respective isoenzymes, leading to new opportunities in diagnosis. On interaction with the enzyme, the naphthoquinone probe undergoes an instantaneous and striking visible color change from red to blue. Spectroscopic, chemical, molecular modelling and biochemical studies reported here show that the color change is mediated by selective recognition between the conjugate base of the sulfonamide group within the probe and the conjugate acid of the arginine residue within the active site of both hNAT1 and mNat2. This represents a new mechanism for selective biomarker sensing and may be exploited as a general approach to the specific detection of biomarkers in disease. |
format | Online Article Text |
id | pubmed-3734253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37342532013-08-12 A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 Laurieri, Nicola Egleton, James E. Varney, Amy Thinnes, Cyrille C. Quevedo, Camilo E. Seden, Peter T. Thompson, Sam Rodrigues-Lima, Fernando Dairou, Julien Dupret, Jean-Marie Russell, Angela J. Sim, Edith PLoS One Research Article Human arylamine N-acetyltransferase 1 (hNAT1) has become an attractive potential biomarker for estrogen-receptor-positive breast cancers. We describe here the mechanism of action of a selective non-covalent colorimetric biosensor for the recognition of hNAT1 and its murine homologue, mNat2, over their respective isoenzymes, leading to new opportunities in diagnosis. On interaction with the enzyme, the naphthoquinone probe undergoes an instantaneous and striking visible color change from red to blue. Spectroscopic, chemical, molecular modelling and biochemical studies reported here show that the color change is mediated by selective recognition between the conjugate base of the sulfonamide group within the probe and the conjugate acid of the arginine residue within the active site of both hNAT1 and mNat2. This represents a new mechanism for selective biomarker sensing and may be exploited as a general approach to the specific detection of biomarkers in disease. Public Library of Science 2013-08-05 /pmc/articles/PMC3734253/ /pubmed/23940600 http://dx.doi.org/10.1371/journal.pone.0070600 Text en © 2013 Laurieri et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Laurieri, Nicola Egleton, James E. Varney, Amy Thinnes, Cyrille C. Quevedo, Camilo E. Seden, Peter T. Thompson, Sam Rodrigues-Lima, Fernando Dairou, Julien Dupret, Jean-Marie Russell, Angela J. Sim, Edith A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 |
title | A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 |
title_full | A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 |
title_fullStr | A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 |
title_full_unstemmed | A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 |
title_short | A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1 |
title_sort | novel color change mechanism for breast cancer biomarker detection: naphthoquinones as specific ligands of human arylamine n-acetyltransferase 1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734253/ https://www.ncbi.nlm.nih.gov/pubmed/23940600 http://dx.doi.org/10.1371/journal.pone.0070600 |
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