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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...

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Autores principales: Fliszár-Nyúl, Eszter, Lemli, Beáta, Kunsági-Máté, Sándor, Dellafiora, Luca, Dall’Asta, Chiara, Cruciani, Gabriele, Pethő, Gábor, Poór, Miklós
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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