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Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers
An enzyme-linked immunosorbent assay that is dependent on enzyme amplification has dominated the current field of protein detection; however, limited multiple detection ability and susceptible enzymatic reactions, and low sensitivity may severely hinder its application. Here, we report a new signal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004922/ https://www.ncbi.nlm.nih.gov/pubmed/29997790 http://dx.doi.org/10.1039/c5sc04256a |
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author | Li, Chao Yang, Yucai Wu, Dan Li, Tianqi Yin, Yongmei Li, Genxi |
author_facet | Li, Chao Yang, Yucai Wu, Dan Li, Tianqi Yin, Yongmei Li, Genxi |
author_sort | Li, Chao |
collection | PubMed |
description | An enzyme-linked immunosorbent assay that is dependent on enzyme amplification has dominated the current field of protein detection; however, limited multiple detection ability and susceptible enzymatic reactions, and low sensitivity may severely hinder its application. Here, we report a new signal amplification scheme based on allochroic molecule modified carboxyl graphene oxide (cGO), which can be used to develop a multicolor immunoassay named as allochroic-cGO linked immunosorbent assay (ALISA). Thanks to high adsorption levels and a wide selection of allochroic molecules, the simultaneous colorimetric detection of diagnostic biomarkers at a picogram level can be successfully achieved for the first time. In addition, the color change triggered by acidic or basic water can provide a simple, rapid, stable and economical signal output, further meeting the growing biodetection requirements. Moreover, with the help of ALISA, we demonstrate that the combined detection of three tumor biomarkers, including carcino-embryonic antigen, neuron-specific enolase, and cytokeratin-19 fragment, is more valuable for differentiating lung cancer patients than the detection of a single biomarker, further manifesting the superiority of ALISA. All in all, this straightforward approach not only opens up new prospects for multicolor immunoassays, but also has great potential for applications in resource-constrained settings. |
format | Online Article Text |
id | pubmed-6004922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60049222018-07-11 Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers Li, Chao Yang, Yucai Wu, Dan Li, Tianqi Yin, Yongmei Li, Genxi Chem Sci Chemistry An enzyme-linked immunosorbent assay that is dependent on enzyme amplification has dominated the current field of protein detection; however, limited multiple detection ability and susceptible enzymatic reactions, and low sensitivity may severely hinder its application. Here, we report a new signal amplification scheme based on allochroic molecule modified carboxyl graphene oxide (cGO), which can be used to develop a multicolor immunoassay named as allochroic-cGO linked immunosorbent assay (ALISA). Thanks to high adsorption levels and a wide selection of allochroic molecules, the simultaneous colorimetric detection of diagnostic biomarkers at a picogram level can be successfully achieved for the first time. In addition, the color change triggered by acidic or basic water can provide a simple, rapid, stable and economical signal output, further meeting the growing biodetection requirements. Moreover, with the help of ALISA, we demonstrate that the combined detection of three tumor biomarkers, including carcino-embryonic antigen, neuron-specific enolase, and cytokeratin-19 fragment, is more valuable for differentiating lung cancer patients than the detection of a single biomarker, further manifesting the superiority of ALISA. All in all, this straightforward approach not only opens up new prospects for multicolor immunoassays, but also has great potential for applications in resource-constrained settings. Royal Society of Chemistry 2016-05-01 2016-02-03 /pmc/articles/PMC6004922/ /pubmed/29997790 http://dx.doi.org/10.1039/c5sc04256a Text en This journal is © The Royal Society of Chemistry 2016 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Li, Chao Yang, Yucai Wu, Dan Li, Tianqi Yin, Yongmei Li, Genxi Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers |
title | Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers
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title_full | Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers
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title_fullStr | Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers
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title_full_unstemmed | Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers
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title_short | Improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers
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title_sort | improvement of enzyme-linked immunosorbent assay for the multicolor detection of biomarkers |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004922/ https://www.ncbi.nlm.nih.gov/pubmed/29997790 http://dx.doi.org/10.1039/c5sc04256a |
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