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Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe

Mitochondria play a critical role in generating energy to support the entire lifecycle of biological cells, yet it is still unclear how their morphological structures evolve to regulate their functionality. Conventional fluorescence microscopy can only provide ~300 nm resolution, which is insufficie...

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Autores principales: Yang, Xusan, Yang, Zhigang, Wu, Zhaoyang, He, Ying, Shan, Chunyan, Chai, Peiyuan, Ma, Chenshuo, Tian, Mi, Teng, Junlin, Jin, Dayong, Yan, Wei, Das, Pintu, Qu, Junle, Xi, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382495/
https://www.ncbi.nlm.nih.gov/pubmed/32709877
http://dx.doi.org/10.1038/s41467-020-17546-1
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author Yang, Xusan
Yang, Zhigang
Wu, Zhaoyang
He, Ying
Shan, Chunyan
Chai, Peiyuan
Ma, Chenshuo
Tian, Mi
Teng, Junlin
Jin, Dayong
Yan, Wei
Das, Pintu
Qu, Junle
Xi, Peng
author_facet Yang, Xusan
Yang, Zhigang
Wu, Zhaoyang
He, Ying
Shan, Chunyan
Chai, Peiyuan
Ma, Chenshuo
Tian, Mi
Teng, Junlin
Jin, Dayong
Yan, Wei
Das, Pintu
Qu, Junle
Xi, Peng
author_sort Yang, Xusan
collection PubMed
description Mitochondria play a critical role in generating energy to support the entire lifecycle of biological cells, yet it is still unclear how their morphological structures evolve to regulate their functionality. Conventional fluorescence microscopy can only provide ~300 nm resolution, which is insufficient to visualize mitochondrial cristae. Here, we developed an enhanced squaraine variant dye (MitoESq-635) to study the dynamic structures of mitochondrial cristae in live cells with a superresolution technique. The low saturation intensity and high photostability of MitoESq-635 make it ideal for long-term, high-resolution (stimulated emission depletion) STED nanoscopy. We performed time-lapse imaging of the mitochondrial inner membrane over 50 min (3.9 s per frame, with 71.5 s dark recovery) in living HeLa cells with a resolution of 35.2 nm. The forms of the cristae during mitochondrial fusion and fission can be clearly observed. Our study demonstrates the emerging capability of optical STED nanoscopy to investigate intracellular physiological processes with nanoscale resolution for an extended period of time.
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spelling pubmed-73824952020-07-28 Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe Yang, Xusan Yang, Zhigang Wu, Zhaoyang He, Ying Shan, Chunyan Chai, Peiyuan Ma, Chenshuo Tian, Mi Teng, Junlin Jin, Dayong Yan, Wei Das, Pintu Qu, Junle Xi, Peng Nat Commun Article Mitochondria play a critical role in generating energy to support the entire lifecycle of biological cells, yet it is still unclear how their morphological structures evolve to regulate their functionality. Conventional fluorescence microscopy can only provide ~300 nm resolution, which is insufficient to visualize mitochondrial cristae. Here, we developed an enhanced squaraine variant dye (MitoESq-635) to study the dynamic structures of mitochondrial cristae in live cells with a superresolution technique. The low saturation intensity and high photostability of MitoESq-635 make it ideal for long-term, high-resolution (stimulated emission depletion) STED nanoscopy. We performed time-lapse imaging of the mitochondrial inner membrane over 50 min (3.9 s per frame, with 71.5 s dark recovery) in living HeLa cells with a resolution of 35.2 nm. The forms of the cristae during mitochondrial fusion and fission can be clearly observed. Our study demonstrates the emerging capability of optical STED nanoscopy to investigate intracellular physiological processes with nanoscale resolution for an extended period of time. Nature Publishing Group UK 2020-07-24 /pmc/articles/PMC7382495/ /pubmed/32709877 http://dx.doi.org/10.1038/s41467-020-17546-1 Text en © The Author(s) 2020 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/.
spellingShingle Article
Yang, Xusan
Yang, Zhigang
Wu, Zhaoyang
He, Ying
Shan, Chunyan
Chai, Peiyuan
Ma, Chenshuo
Tian, Mi
Teng, Junlin
Jin, Dayong
Yan, Wei
Das, Pintu
Qu, Junle
Xi, Peng
Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe
title Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe
title_full Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe
title_fullStr Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe
title_full_unstemmed Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe
title_short Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe
title_sort mitochondrial dynamics quantitatively revealed by sted nanoscopy with an enhanced squaraine variant probe
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382495/
https://www.ncbi.nlm.nih.gov/pubmed/32709877
http://dx.doi.org/10.1038/s41467-020-17546-1
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