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The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro

The molybdenum cluster [Mo(6)Cl(14)](2−) is a fluorescent component with potential for use in cell labelling and pharmacology. Biological safety and antiviral properties of the cluster are as yet unknown. Here, we show the effect of acute exposition of human cells and red blood cells to the molybden...

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Autores principales: Rojas-Mancilla, Edgardo, Oyarce, Alexis, Verdugo, Viviana, Morales-Verdejo, Cesar, Echeverria, Cesar, Velásquez, Felipe, Chnaiderman, Jonas, Valiente-Echeverría, Fernando, Ramirez-Tagle, Rodrigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152029/
https://www.ncbi.nlm.nih.gov/pubmed/28678175
http://dx.doi.org/10.3390/molecules22071108
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author Rojas-Mancilla, Edgardo
Oyarce, Alexis
Verdugo, Viviana
Morales-Verdejo, Cesar
Echeverria, Cesar
Velásquez, Felipe
Chnaiderman, Jonas
Valiente-Echeverría, Fernando
Ramirez-Tagle, Rodrigo
author_facet Rojas-Mancilla, Edgardo
Oyarce, Alexis
Verdugo, Viviana
Morales-Verdejo, Cesar
Echeverria, Cesar
Velásquez, Felipe
Chnaiderman, Jonas
Valiente-Echeverría, Fernando
Ramirez-Tagle, Rodrigo
author_sort Rojas-Mancilla, Edgardo
collection PubMed
description The molybdenum cluster [Mo(6)Cl(14)](2−) is a fluorescent component with potential for use in cell labelling and pharmacology. Biological safety and antiviral properties of the cluster are as yet unknown. Here, we show the effect of acute exposition of human cells and red blood cells to the molybdenum cluster and its interaction with proteins and antiviral activity in vitro. We measured cell viability of HepG2 and EA.hy926 cell lines exposed to increasing concentrations of the cluster (0.1 to 250 µM), by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. Hemolysis and morphological alterations of red blood cells, obtained from healthy donors, exposed to the cluster (10 to 200 µM) at 37 °C were analyzed. Furthermore, quenching of tryptophan residues of albumin was performed. Finally, plaque formation by rotavirus SA11 in MA104 cells treated with the cluster (100 to 300 µM) were analyzed. We found that all doses of the cluster showed similar cell viability, hemolysis, and morphology values, compared to control. Quenching of tryptophan residues of albumin suggests a protein-cluster complex formation. Finally, the cluster showed antiviral activity at 300 µM. These results indicate that the cluster [Mo(6)Cl(14)](2−) could be intravenously administered in animals at therapeutic doses for further in vivo studies and might be studied as an antiviral agent.
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spelling pubmed-61520292018-11-13 The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro Rojas-Mancilla, Edgardo Oyarce, Alexis Verdugo, Viviana Morales-Verdejo, Cesar Echeverria, Cesar Velásquez, Felipe Chnaiderman, Jonas Valiente-Echeverría, Fernando Ramirez-Tagle, Rodrigo Molecules Article The molybdenum cluster [Mo(6)Cl(14)](2−) is a fluorescent component with potential for use in cell labelling and pharmacology. Biological safety and antiviral properties of the cluster are as yet unknown. Here, we show the effect of acute exposition of human cells and red blood cells to the molybdenum cluster and its interaction with proteins and antiviral activity in vitro. We measured cell viability of HepG2 and EA.hy926 cell lines exposed to increasing concentrations of the cluster (0.1 to 250 µM), by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. Hemolysis and morphological alterations of red blood cells, obtained from healthy donors, exposed to the cluster (10 to 200 µM) at 37 °C were analyzed. Furthermore, quenching of tryptophan residues of albumin was performed. Finally, plaque formation by rotavirus SA11 in MA104 cells treated with the cluster (100 to 300 µM) were analyzed. We found that all doses of the cluster showed similar cell viability, hemolysis, and morphology values, compared to control. Quenching of tryptophan residues of albumin suggests a protein-cluster complex formation. Finally, the cluster showed antiviral activity at 300 µM. These results indicate that the cluster [Mo(6)Cl(14)](2−) could be intravenously administered in animals at therapeutic doses for further in vivo studies and might be studied as an antiviral agent. MDPI 2017-07-05 /pmc/articles/PMC6152029/ /pubmed/28678175 http://dx.doi.org/10.3390/molecules22071108 Text en © 2017 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
Rojas-Mancilla, Edgardo
Oyarce, Alexis
Verdugo, Viviana
Morales-Verdejo, Cesar
Echeverria, Cesar
Velásquez, Felipe
Chnaiderman, Jonas
Valiente-Echeverría, Fernando
Ramirez-Tagle, Rodrigo
The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro
title The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro
title_full The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro
title_fullStr The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro
title_full_unstemmed The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro
title_short The [Mo(6)Cl(14)](2−) Cluster is Biologically Secure and Has Anti-Rotavirus Activity In Vitro
title_sort [mo(6)cl(14)](2−) cluster is biologically secure and has anti-rotavirus activity in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152029/
https://www.ncbi.nlm.nih.gov/pubmed/28678175
http://dx.doi.org/10.3390/molecules22071108
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