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Interaction of Mycotoxin Alternariol with Serum Albumin
Alternariol (AOH) is a mycotoxin produced by Alternaria species. In vitro studies suggest the genotoxic, mutagenic, and endocrine disruptor effects of AOH, and an increased incidence of esophageal cancer has been reported related to higher AOH exposure. Human serum albumin (HSA) is the most abundant...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539399/ https://www.ncbi.nlm.nih.gov/pubmed/31083629 http://dx.doi.org/10.3390/ijms20092352 |
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author | Fliszár-Nyúl, Eszter Lemli, Beáta Kunsági-Máté, Sándor Dellafiora, Luca Dall’Asta, Chiara Cruciani, Gabriele Pethő, Gábor Poór, Miklós |
author_facet | Fliszár-Nyúl, Eszter Lemli, Beáta Kunsági-Máté, Sándor Dellafiora, Luca Dall’Asta, Chiara Cruciani, Gabriele Pethő, Gábor Poór, Miklós |
author_sort | Fliszár-Nyúl, Eszter |
collection | PubMed |
description | Alternariol (AOH) is a mycotoxin produced by Alternaria species. In vitro studies suggest the genotoxic, mutagenic, and endocrine disruptor effects of AOH, and an increased incidence of esophageal cancer has been reported related to higher AOH exposure. Human serum albumin (HSA) is the most abundant plasma protein in the circulation, it is able to affect toxicokinetic properties of numerous xenobiotics. HSA forms stable complexes with several mycotoxins, however, the interaction of AOH with albumin has not been examined. In this study, the complex formation of AOH with HSA was tested, employing fluorescence spectroscopy, ultrafiltration, and molecular modeling. Each spectroscopic measurement shows the formation of stable AOH-HSA complexes (K = 4 × 10(5) L/mol). Investigations with site markers (in spectroscopic and ultrafiltration models) as well as modeling studies suggest that AOH occupies Sudlow’s site I as a high-affinity binding site in HSA. The binding affinity of AOH towards bovine, porcine, and rat albumins was also tested, suggesting that AOH binds to rat albumin with considerably higher affinity than other albumins tested. Our results demonstrate the strong interaction of AOH with serum albumins, suggesting the potential in vivo importance of these interactions. |
format | Online Article Text |
id | pubmed-6539399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65393992019-06-04 Interaction of Mycotoxin Alternariol with Serum Albumin Fliszár-Nyúl, Eszter Lemli, Beáta Kunsági-Máté, Sándor Dellafiora, Luca Dall’Asta, Chiara Cruciani, Gabriele Pethő, Gábor Poór, Miklós Int J Mol Sci Article Alternariol (AOH) is a mycotoxin produced by Alternaria species. In vitro studies suggest the genotoxic, mutagenic, and endocrine disruptor effects of AOH, and an increased incidence of esophageal cancer has been reported related to higher AOH exposure. Human serum albumin (HSA) is the most abundant plasma protein in the circulation, it is able to affect toxicokinetic properties of numerous xenobiotics. HSA forms stable complexes with several mycotoxins, however, the interaction of AOH with albumin has not been examined. In this study, the complex formation of AOH with HSA was tested, employing fluorescence spectroscopy, ultrafiltration, and molecular modeling. Each spectroscopic measurement shows the formation of stable AOH-HSA complexes (K = 4 × 10(5) L/mol). Investigations with site markers (in spectroscopic and ultrafiltration models) as well as modeling studies suggest that AOH occupies Sudlow’s site I as a high-affinity binding site in HSA. The binding affinity of AOH towards bovine, porcine, and rat albumins was also tested, suggesting that AOH binds to rat albumin with considerably higher affinity than other albumins tested. Our results demonstrate the strong interaction of AOH with serum albumins, suggesting the potential in vivo importance of these interactions. MDPI 2019-05-12 /pmc/articles/PMC6539399/ /pubmed/31083629 http://dx.doi.org/10.3390/ijms20092352 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fliszár-Nyúl, Eszter Lemli, Beáta Kunsági-Máté, Sándor Dellafiora, Luca Dall’Asta, Chiara Cruciani, Gabriele Pethő, Gábor Poór, Miklós Interaction of Mycotoxin Alternariol with Serum Albumin |
title | Interaction of Mycotoxin Alternariol with Serum Albumin |
title_full | Interaction of Mycotoxin Alternariol with Serum Albumin |
title_fullStr | Interaction of Mycotoxin Alternariol with Serum Albumin |
title_full_unstemmed | Interaction of Mycotoxin Alternariol with Serum Albumin |
title_short | Interaction of Mycotoxin Alternariol with Serum Albumin |
title_sort | interaction of mycotoxin alternariol with serum albumin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539399/ https://www.ncbi.nlm.nih.gov/pubmed/31083629 http://dx.doi.org/10.3390/ijms20092352 |
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