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Two-photon activated precision molecular photosensitizer targeting mitochondria
Mitochondria metabolism is an emergent target for the development of novel anticancer agents. It is amply recognized that strategies that allow for modulation of mitochondrial function in specific cell populations need to be developed for the therapeutic potential of mitochondria-targeting agents to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814857/ https://www.ncbi.nlm.nih.gov/pubmed/36697839 http://dx.doi.org/10.1038/s42004-021-00581-4 |
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author | Mariz, Inês F. A. Pinto, Sandra N. Santiago, Ana M. Martinho, José M. G. Recio, Javier Vaquero, Juan J. Cuadro, Ana M. Maçôas, Ermelinda |
author_facet | Mariz, Inês F. A. Pinto, Sandra N. Santiago, Ana M. Martinho, José M. G. Recio, Javier Vaquero, Juan J. Cuadro, Ana M. Maçôas, Ermelinda |
author_sort | Mariz, Inês F. A. |
collection | PubMed |
description | Mitochondria metabolism is an emergent target for the development of novel anticancer agents. It is amply recognized that strategies that allow for modulation of mitochondrial function in specific cell populations need to be developed for the therapeutic potential of mitochondria-targeting agents to become a reality in the clinic. In this work, we report dipolar and quadrupolar quinolizinium and benzimidazolium cations that show mitochondria targeting ability and localized light-induced mitochondria damage in live animal cells. Some of the dyes induce a very efficient disruption of mitochondrial potential and subsequent cell death under two-photon excitation in the Near-infrared (NIR) opening up possible applications of azonia/azolium aromatic heterocycles as precision photosensitizers. The dipolar compounds could be excited in the NIR due to a high two-photon brightness while exhibiting emission in the red part of the visible spectra (600–700 nm). Interaction with the mitochondria leads to an unexpected blue-shift of the emission of the far-red emitting compounds, which we assign to emission from the locally excited state. Interaction and possibly aggregation at the mitochondria prevents access to the intramolecular charge transfer state responsible for far-red emission. |
format | Online Article Text |
id | pubmed-9814857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98148572023-01-10 Two-photon activated precision molecular photosensitizer targeting mitochondria Mariz, Inês F. A. Pinto, Sandra N. Santiago, Ana M. Martinho, José M. G. Recio, Javier Vaquero, Juan J. Cuadro, Ana M. Maçôas, Ermelinda Commun Chem Article Mitochondria metabolism is an emergent target for the development of novel anticancer agents. It is amply recognized that strategies that allow for modulation of mitochondrial function in specific cell populations need to be developed for the therapeutic potential of mitochondria-targeting agents to become a reality in the clinic. In this work, we report dipolar and quadrupolar quinolizinium and benzimidazolium cations that show mitochondria targeting ability and localized light-induced mitochondria damage in live animal cells. Some of the dyes induce a very efficient disruption of mitochondrial potential and subsequent cell death under two-photon excitation in the Near-infrared (NIR) opening up possible applications of azonia/azolium aromatic heterocycles as precision photosensitizers. The dipolar compounds could be excited in the NIR due to a high two-photon brightness while exhibiting emission in the red part of the visible spectra (600–700 nm). Interaction with the mitochondria leads to an unexpected blue-shift of the emission of the far-red emitting compounds, which we assign to emission from the locally excited state. Interaction and possibly aggregation at the mitochondria prevents access to the intramolecular charge transfer state responsible for far-red emission. Nature Publishing Group UK 2021-10-07 /pmc/articles/PMC9814857/ /pubmed/36697839 http://dx.doi.org/10.1038/s42004-021-00581-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mariz, Inês F. A. Pinto, Sandra N. Santiago, Ana M. Martinho, José M. G. Recio, Javier Vaquero, Juan J. Cuadro, Ana M. Maçôas, Ermelinda Two-photon activated precision molecular photosensitizer targeting mitochondria |
title | Two-photon activated precision molecular photosensitizer targeting mitochondria |
title_full | Two-photon activated precision molecular photosensitizer targeting mitochondria |
title_fullStr | Two-photon activated precision molecular photosensitizer targeting mitochondria |
title_full_unstemmed | Two-photon activated precision molecular photosensitizer targeting mitochondria |
title_short | Two-photon activated precision molecular photosensitizer targeting mitochondria |
title_sort | two-photon activated precision molecular photosensitizer targeting mitochondria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814857/ https://www.ncbi.nlm.nih.gov/pubmed/36697839 http://dx.doi.org/10.1038/s42004-021-00581-4 |
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