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Application of BisANS fluorescent dye for developing a novel protein assay
In many biology- and chemistry-related research fields and experiments the quantification of the peptide and/or protein concentration in samples are essential. Every research environment has unique requirements, e.g. metal ions, incubation times, photostability, pH, protease inhibitors, chelators, d...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474611/ https://www.ncbi.nlm.nih.gov/pubmed/31002721 http://dx.doi.org/10.1371/journal.pone.0215863 |
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author | Datki, Zsolt Olah, Zita Macsai, Lilla Pakaski, Magdolna Galik, Bence Mihaly, Gabor Kalman, Janos |
author_facet | Datki, Zsolt Olah, Zita Macsai, Lilla Pakaski, Magdolna Galik, Bence Mihaly, Gabor Kalman, Janos |
author_sort | Datki, Zsolt |
collection | PubMed |
description | In many biology- and chemistry-related research fields and experiments the quantification of the peptide and/or protein concentration in samples are essential. Every research environment has unique requirements, e.g. metal ions, incubation times, photostability, pH, protease inhibitors, chelators, detergents, etc. A new protein assay may be adequate in different experiments beyond or instead of the well-known standard protocols (e.g. Qubit, Bradford or bicinchoninic acid) in related conceptions. Based on our previous studies, we developed a novel protein assay applying the 4,4′-Dianilino-1,1′-binaphthyl-5,5′-disulfonic acid dipotassium salt (BisANS) fluorescent dye. This molecule has several advantageous properties related to protein detection: good solubility in water, high photostability at adequate pH, quick interaction kinetics (within seconds) with proteins and no exclusionary sensitivity to the chelator, detergent and inhibitor ingredients. The protocol described in this work is highly sensitive in a large spectrum to detect protein (100-fold diluted samples) concentrations (from 0.28 up to more than 100 μg/mL). The BisANS protein assay is valid and applicable for quantification of the amount of protein in different biological and/or chemical samples. |
format | Online Article Text |
id | pubmed-6474611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64746112019-05-03 Application of BisANS fluorescent dye for developing a novel protein assay Datki, Zsolt Olah, Zita Macsai, Lilla Pakaski, Magdolna Galik, Bence Mihaly, Gabor Kalman, Janos PLoS One Research Article In many biology- and chemistry-related research fields and experiments the quantification of the peptide and/or protein concentration in samples are essential. Every research environment has unique requirements, e.g. metal ions, incubation times, photostability, pH, protease inhibitors, chelators, detergents, etc. A new protein assay may be adequate in different experiments beyond or instead of the well-known standard protocols (e.g. Qubit, Bradford or bicinchoninic acid) in related conceptions. Based on our previous studies, we developed a novel protein assay applying the 4,4′-Dianilino-1,1′-binaphthyl-5,5′-disulfonic acid dipotassium salt (BisANS) fluorescent dye. This molecule has several advantageous properties related to protein detection: good solubility in water, high photostability at adequate pH, quick interaction kinetics (within seconds) with proteins and no exclusionary sensitivity to the chelator, detergent and inhibitor ingredients. The protocol described in this work is highly sensitive in a large spectrum to detect protein (100-fold diluted samples) concentrations (from 0.28 up to more than 100 μg/mL). The BisANS protein assay is valid and applicable for quantification of the amount of protein in different biological and/or chemical samples. Public Library of Science 2019-04-19 /pmc/articles/PMC6474611/ /pubmed/31002721 http://dx.doi.org/10.1371/journal.pone.0215863 Text en © 2019 Datki 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Datki, Zsolt Olah, Zita Macsai, Lilla Pakaski, Magdolna Galik, Bence Mihaly, Gabor Kalman, Janos Application of BisANS fluorescent dye for developing a novel protein assay |
title | Application of BisANS fluorescent dye for developing a novel protein assay |
title_full | Application of BisANS fluorescent dye for developing a novel protein assay |
title_fullStr | Application of BisANS fluorescent dye for developing a novel protein assay |
title_full_unstemmed | Application of BisANS fluorescent dye for developing a novel protein assay |
title_short | Application of BisANS fluorescent dye for developing a novel protein assay |
title_sort | application of bisans fluorescent dye for developing a novel protein assay |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474611/ https://www.ncbi.nlm.nih.gov/pubmed/31002721 http://dx.doi.org/10.1371/journal.pone.0215863 |
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