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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...

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Autores principales: Datki, Zsolt, Olah, Zita, Macsai, Lilla, Pakaski, Magdolna, Galik, Bence, Mihaly, Gabor, Kalman, Janos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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