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Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and imaging in live zebrafish
Hydrogen sulfide (H(2)S) is an important biological messenger, but few biologically-compatible methods are available for its detection in aqueous solution. Herein, we report a highly water-soluble naphthalimide-based fluorescent probe (L(1)), which is a highly versatile building unit that absorbs an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870630/ https://www.ncbi.nlm.nih.gov/pubmed/27188400 http://dx.doi.org/10.1038/srep26203 |
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author | Choi, Seon-Ae Park, Chul Soon Kwon, Oh Seok Giong, Hoi-Khoanh Lee, Jeong-Soo Ha, Tai Hwan Lee, Chang-Soo |
author_facet | Choi, Seon-Ae Park, Chul Soon Kwon, Oh Seok Giong, Hoi-Khoanh Lee, Jeong-Soo Ha, Tai Hwan Lee, Chang-Soo |
author_sort | Choi, Seon-Ae |
collection | PubMed |
description | Hydrogen sulfide (H(2)S) is an important biological messenger, but few biologically-compatible methods are available for its detection in aqueous solution. Herein, we report a highly water-soluble naphthalimide-based fluorescent probe (L(1)), which is a highly versatile building unit that absorbs and emits at long wavelengths and is selective for hydrogen sulfide over cysteine, glutathione, and other reactive sulfur, nitrogen, and oxygen species in aqueous solution. We describe turn-on fluorescent probes based on azide group reduction on the fluorogenic ‘naphthalene’ moiety to fluorescent amines and intracellular hydrogen sulfide detection without the use of an organic solvent. L(1) and L(2) were synthetically modified to functional groups with comparable solubility on the N-imide site, showing a marked change in turn-on fluorescent intensity in response to hydrogen sulfide in both PBS buffer and living cells. The probes were readily employed to assess intracellular hydrogen sulfide level changes by imaging endogenous hydrogen sulfide signal in RAW264.7 cells incubated with L(1) and L(2). Expanding the use of L(1) to complex and heterogeneous biological settings, we successfully visualized hydrogen sulfide detection in the yolk, brain and spinal cord of living zebrafish embryos, thereby providing a powerful approach for live imaging for investigating chemical signaling in complex multicellular systems. |
format | Online Article Text |
id | pubmed-4870630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48706302016-06-01 Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and imaging in live zebrafish Choi, Seon-Ae Park, Chul Soon Kwon, Oh Seok Giong, Hoi-Khoanh Lee, Jeong-Soo Ha, Tai Hwan Lee, Chang-Soo Sci Rep Article Hydrogen sulfide (H(2)S) is an important biological messenger, but few biologically-compatible methods are available for its detection in aqueous solution. Herein, we report a highly water-soluble naphthalimide-based fluorescent probe (L(1)), which is a highly versatile building unit that absorbs and emits at long wavelengths and is selective for hydrogen sulfide over cysteine, glutathione, and other reactive sulfur, nitrogen, and oxygen species in aqueous solution. We describe turn-on fluorescent probes based on azide group reduction on the fluorogenic ‘naphthalene’ moiety to fluorescent amines and intracellular hydrogen sulfide detection without the use of an organic solvent. L(1) and L(2) were synthetically modified to functional groups with comparable solubility on the N-imide site, showing a marked change in turn-on fluorescent intensity in response to hydrogen sulfide in both PBS buffer and living cells. The probes were readily employed to assess intracellular hydrogen sulfide level changes by imaging endogenous hydrogen sulfide signal in RAW264.7 cells incubated with L(1) and L(2). Expanding the use of L(1) to complex and heterogeneous biological settings, we successfully visualized hydrogen sulfide detection in the yolk, brain and spinal cord of living zebrafish embryos, thereby providing a powerful approach for live imaging for investigating chemical signaling in complex multicellular systems. Nature Publishing Group 2016-05-18 /pmc/articles/PMC4870630/ /pubmed/27188400 http://dx.doi.org/10.1038/srep26203 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 Choi, Seon-Ae Park, Chul Soon Kwon, Oh Seok Giong, Hoi-Khoanh Lee, Jeong-Soo Ha, Tai Hwan Lee, Chang-Soo Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and imaging in live zebrafish |
title | Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and
imaging in live zebrafish |
title_full | Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and
imaging in live zebrafish |
title_fullStr | Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and
imaging in live zebrafish |
title_full_unstemmed | Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and
imaging in live zebrafish |
title_short | Structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and
imaging in live zebrafish |
title_sort | structural effects of naphthalimide-based fluorescent sensor for hydrogen sulfide and
imaging in live zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870630/ https://www.ncbi.nlm.nih.gov/pubmed/27188400 http://dx.doi.org/10.1038/srep26203 |
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