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The Interaction of Hypericin with SARS-CoV-2 Reveals a Multimodal Antiviral Activity
[Image: see text] Hypericin is a photosensitizing drug that is active against membrane-enveloped viruses and therefore constitutes a promising candidate for the treatment of SARS-CoV-2 infections. The antiviral efficacy of hypericin is largely determined by its affinity toward viral components and b...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972258/ https://www.ncbi.nlm.nih.gov/pubmed/35302731 http://dx.doi.org/10.1021/acsami.1c22439 |
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author | Delcanale, Pietro Uriati, Eleonora Mariangeli, Matteo Mussini, Andrea Moreno, Ana Lelli, Davide Cavanna, Luigi Bianchini, Paolo Diaspro, Alberto Abbruzzetti, Stefania Viappiani, Cristiano |
author_facet | Delcanale, Pietro Uriati, Eleonora Mariangeli, Matteo Mussini, Andrea Moreno, Ana Lelli, Davide Cavanna, Luigi Bianchini, Paolo Diaspro, Alberto Abbruzzetti, Stefania Viappiani, Cristiano |
author_sort | Delcanale, Pietro |
collection | PubMed |
description | [Image: see text] Hypericin is a photosensitizing drug that is active against membrane-enveloped viruses and therefore constitutes a promising candidate for the treatment of SARS-CoV-2 infections. The antiviral efficacy of hypericin is largely determined by its affinity toward viral components and by the number of active molecules loaded on single viruses. Here we use an experimental approach to follow the interaction of hypericin with SARS-CoV-2, and we evaluate its antiviral efficacy, both in the dark and upon photoactivation. Binding to viral particles is directly visualized with fluorescence microscopy, and a strong affinity for the viral particles, most likely for the viral envelope, is measured spectroscopically. The loading of a maximum of approximately 30 molecules per viral particle is estimated, despite with marked heterogeneity among particles. Because of this interaction, nanomolar concentrations of photoactivated hypericin substantially reduce virus infectivity on Vero E6 cells, but a partial effect is also observed in dark conditions, suggesting multiple mechanisms of action for this drug. |
format | Online Article Text |
id | pubmed-8972258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89722582022-04-01 The Interaction of Hypericin with SARS-CoV-2 Reveals a Multimodal Antiviral Activity Delcanale, Pietro Uriati, Eleonora Mariangeli, Matteo Mussini, Andrea Moreno, Ana Lelli, Davide Cavanna, Luigi Bianchini, Paolo Diaspro, Alberto Abbruzzetti, Stefania Viappiani, Cristiano ACS Appl Mater Interfaces [Image: see text] Hypericin is a photosensitizing drug that is active against membrane-enveloped viruses and therefore constitutes a promising candidate for the treatment of SARS-CoV-2 infections. The antiviral efficacy of hypericin is largely determined by its affinity toward viral components and by the number of active molecules loaded on single viruses. Here we use an experimental approach to follow the interaction of hypericin with SARS-CoV-2, and we evaluate its antiviral efficacy, both in the dark and upon photoactivation. Binding to viral particles is directly visualized with fluorescence microscopy, and a strong affinity for the viral particles, most likely for the viral envelope, is measured spectroscopically. The loading of a maximum of approximately 30 molecules per viral particle is estimated, despite with marked heterogeneity among particles. Because of this interaction, nanomolar concentrations of photoactivated hypericin substantially reduce virus infectivity on Vero E6 cells, but a partial effect is also observed in dark conditions, suggesting multiple mechanisms of action for this drug. American Chemical Society 2022-03-18 2022-03-30 /pmc/articles/PMC8972258/ /pubmed/35302731 http://dx.doi.org/10.1021/acsami.1c22439 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Delcanale, Pietro Uriati, Eleonora Mariangeli, Matteo Mussini, Andrea Moreno, Ana Lelli, Davide Cavanna, Luigi Bianchini, Paolo Diaspro, Alberto Abbruzzetti, Stefania Viappiani, Cristiano The Interaction of Hypericin with SARS-CoV-2 Reveals a Multimodal Antiviral Activity |
title | The
Interaction of Hypericin with SARS-CoV-2
Reveals a Multimodal Antiviral Activity |
title_full | The
Interaction of Hypericin with SARS-CoV-2
Reveals a Multimodal Antiviral Activity |
title_fullStr | The
Interaction of Hypericin with SARS-CoV-2
Reveals a Multimodal Antiviral Activity |
title_full_unstemmed | The
Interaction of Hypericin with SARS-CoV-2
Reveals a Multimodal Antiviral Activity |
title_short | The
Interaction of Hypericin with SARS-CoV-2
Reveals a Multimodal Antiviral Activity |
title_sort | the
interaction of hypericin with sars-cov-2
reveals a multimodal antiviral activity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972258/ https://www.ncbi.nlm.nih.gov/pubmed/35302731 http://dx.doi.org/10.1021/acsami.1c22439 |
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