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Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products
Cycopiazonic acid (CPA) is a neurotoxin that acts through inhibition of the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA). CPA blocks the calcium access channel of the enzyme. The inhibition may involve the binding of CPA with a divalent cation such as Mg(2+). The potential for CPA to act as a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071049/ https://www.ncbi.nlm.nih.gov/pubmed/29996475 http://dx.doi.org/10.3390/toxins10070285 |
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author | Maragos, Chris M. |
author_facet | Maragos, Chris M. |
author_sort | Maragos, Chris M. |
collection | PubMed |
description | Cycopiazonic acid (CPA) is a neurotoxin that acts through inhibition of the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA). CPA blocks the calcium access channel of the enzyme. The inhibition may involve the binding of CPA with a divalent cation such as Mg(2+). The potential for CPA to act as a chelator also has implications for methods to detect this toxin. Certain of the lanthanide metals undergo a dramatic increase in luminescence upon coordination with small molecules that can transfer excitation energy to the metal. This report is the first to describe the coordination of CPA with lanthanide metals, resulting in a substantial enhancement of their luminescence. The luminescence expressed was dependent upon the type of lanthanide, its concentration, and the environment (solvent, water content, pH). Based upon the phenomenon, a competitive assay was also developed wherein terbium (Tb(3+)) and a series of metal cations competed for binding with CPA. With increasing cation concentration, the luminescence of the CPA/Tb(3+) complex was inhibited. The chlorides of ten metals were tested. Inhibition was best with Cu(2+), followed by Co(2+), Al(3+), Fe(3+), Mn(2+), Au(3+), Mg(2+), and Ca(2+). Two cations in oxidation state one (Na(+), K(+)) did not inhibit the interaction significantly. The interaction of CPA with lanthanides provides a novel recognition assay for this toxin. It also provides a novel way to probe the binding of CPA to metals, giving insights into CPA’s mechanism of action. |
format | Online Article Text |
id | pubmed-6071049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60710492018-08-09 Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products Maragos, Chris M. Toxins (Basel) Article Cycopiazonic acid (CPA) is a neurotoxin that acts through inhibition of the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA). CPA blocks the calcium access channel of the enzyme. The inhibition may involve the binding of CPA with a divalent cation such as Mg(2+). The potential for CPA to act as a chelator also has implications for methods to detect this toxin. Certain of the lanthanide metals undergo a dramatic increase in luminescence upon coordination with small molecules that can transfer excitation energy to the metal. This report is the first to describe the coordination of CPA with lanthanide metals, resulting in a substantial enhancement of their luminescence. The luminescence expressed was dependent upon the type of lanthanide, its concentration, and the environment (solvent, water content, pH). Based upon the phenomenon, a competitive assay was also developed wherein terbium (Tb(3+)) and a series of metal cations competed for binding with CPA. With increasing cation concentration, the luminescence of the CPA/Tb(3+) complex was inhibited. The chlorides of ten metals were tested. Inhibition was best with Cu(2+), followed by Co(2+), Al(3+), Fe(3+), Mn(2+), Au(3+), Mg(2+), and Ca(2+). Two cations in oxidation state one (Na(+), K(+)) did not inhibit the interaction significantly. The interaction of CPA with lanthanides provides a novel recognition assay for this toxin. It also provides a novel way to probe the binding of CPA to metals, giving insights into CPA’s mechanism of action. MDPI 2018-07-10 /pmc/articles/PMC6071049/ /pubmed/29996475 http://dx.doi.org/10.3390/toxins10070285 Text en © 2018 by the author. 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 Maragos, Chris M. Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products |
title | Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products |
title_full | Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products |
title_fullStr | Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products |
title_full_unstemmed | Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products |
title_short | Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products |
title_sort | complexation of the mycotoxin cyclopiazonic acid with lanthanides yields luminescent products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071049/ https://www.ncbi.nlm.nih.gov/pubmed/29996475 http://dx.doi.org/10.3390/toxins10070285 |
work_keys_str_mv | AT maragoschrism complexationofthemycotoxincyclopiazonicacidwithlanthanidesyieldsluminescentproducts |