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A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues

Lysosome-specific fluorescent probes are exclusive to elucidate the functions of lysosomal thiols. Moreover, two-photon microscopy offers advantages of less phototoxicity, better three dimensional spatial localization, deeper penetration depth and lower self-absorption. However, such fluorescent pro...

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Detalles Bibliográficos
Autores principales: Fan, Jiangli, Han, Zhichao, Kang, Yao, Peng, Xiaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726187/
https://www.ncbi.nlm.nih.gov/pubmed/26794434
http://dx.doi.org/10.1038/srep19562
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author Fan, Jiangli
Han, Zhichao
Kang, Yao
Peng, Xiaojun
author_facet Fan, Jiangli
Han, Zhichao
Kang, Yao
Peng, Xiaojun
author_sort Fan, Jiangli
collection PubMed
description Lysosome-specific fluorescent probes are exclusive to elucidate the functions of lysosomal thiols. Moreover, two-photon microscopy offers advantages of less phototoxicity, better three dimensional spatial localization, deeper penetration depth and lower self-absorption. However, such fluorescent probes for thiols are still rare. In this work, an efficient two-photon fluorophore 1,8-naphthalimide-based probe conjugating a 2,4-dinitrobenzenesulfonyl chloride and morpholine was designed and synthesized, which exhibited high selectivity and sensitivity towards lysosomal thiols by turn-on fluorescence method quantitatively and was successfully applied to the imaging of thiols in live cells and tissues by two-photon microscopy.
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spelling pubmed-47261872016-01-27 A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues Fan, Jiangli Han, Zhichao Kang, Yao Peng, Xiaojun Sci Rep Article Lysosome-specific fluorescent probes are exclusive to elucidate the functions of lysosomal thiols. Moreover, two-photon microscopy offers advantages of less phototoxicity, better three dimensional spatial localization, deeper penetration depth and lower self-absorption. However, such fluorescent probes for thiols are still rare. In this work, an efficient two-photon fluorophore 1,8-naphthalimide-based probe conjugating a 2,4-dinitrobenzenesulfonyl chloride and morpholine was designed and synthesized, which exhibited high selectivity and sensitivity towards lysosomal thiols by turn-on fluorescence method quantitatively and was successfully applied to the imaging of thiols in live cells and tissues by two-photon microscopy. Nature Publishing Group 2016-01-22 /pmc/articles/PMC4726187/ /pubmed/26794434 http://dx.doi.org/10.1038/srep19562 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Fan, Jiangli
Han, Zhichao
Kang, Yao
Peng, Xiaojun
A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues
title A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues
title_full A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues
title_fullStr A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues
title_full_unstemmed A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues
title_short A Two-Photon Fluorescent Probe for Lysosomal Thiols in Live Cells and Tissues
title_sort two-photon fluorescent probe for lysosomal thiols in live cells and tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726187/
https://www.ncbi.nlm.nih.gov/pubmed/26794434
http://dx.doi.org/10.1038/srep19562
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