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A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo
Hydrogen sulfide (H(2)S) has been recognized as an important endogenous gasotransmitter associated with biological signaling transduction. However, recent biological studies implied that the H(2)S-related cellular signaling might actually be mediated by hydrogen polysulfides (H(2)S(n), n > 1), no...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050607/ https://www.ncbi.nlm.nih.gov/pubmed/30061987 http://dx.doi.org/10.1039/c8sc01879k |
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author | Yang, Fan Gao, He Li, Shan-Shan An, Rui-Bing Sun, Xiao-Yang Kang, Bin Xu, Jing-Juan Chen, Hong-Yuan |
author_facet | Yang, Fan Gao, He Li, Shan-Shan An, Rui-Bing Sun, Xiao-Yang Kang, Bin Xu, Jing-Juan Chen, Hong-Yuan |
author_sort | Yang, Fan |
collection | PubMed |
description | Hydrogen sulfide (H(2)S) has been recognized as an important endogenous gasotransmitter associated with biological signaling transduction. However, recent biological studies implied that the H(2)S-related cellular signaling might actually be mediated by hydrogen polysulfides (H(2)S(n), n > 1), not H(2)S itself. Unraveling such a mystery strongly demanded the quantification of endogenous H(2)S(n) in living systems. However, endogenous H(2)S(n) has been undetectable thus far, due to its extremely low concentration within cells. Herein, we demonstrated a strategy to detect ultra-trace endogenous H(2)S(n)via a fluorescent τ-probe, through changes of fluorescence lifetime instead of fluorescence intensity. This τ-probe exhibited an ultrasensitive response to H(2)S(n), bringing about the lowest value of the detection limit (2 nM) and a lower limit of quantification (10 nM) to date. With such merits, we quantified and mapped endogenous H(2)S(n) within cells and zebrafish. The quantitative information about endogenous H(2)S(n) in cells and in vivo may have a significant implication for future research on the role of H(2)S(n) in biology. The methodology of the τ-probe established here might provide a general insight into the design and application of any fluorescent probes, beyond the limit of utilizing fluorescence intensity. |
format | Online Article Text |
id | pubmed-6050607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60506072018-07-30 A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo Yang, Fan Gao, He Li, Shan-Shan An, Rui-Bing Sun, Xiao-Yang Kang, Bin Xu, Jing-Juan Chen, Hong-Yuan Chem Sci Chemistry Hydrogen sulfide (H(2)S) has been recognized as an important endogenous gasotransmitter associated with biological signaling transduction. However, recent biological studies implied that the H(2)S-related cellular signaling might actually be mediated by hydrogen polysulfides (H(2)S(n), n > 1), not H(2)S itself. Unraveling such a mystery strongly demanded the quantification of endogenous H(2)S(n) in living systems. However, endogenous H(2)S(n) has been undetectable thus far, due to its extremely low concentration within cells. Herein, we demonstrated a strategy to detect ultra-trace endogenous H(2)S(n)via a fluorescent τ-probe, through changes of fluorescence lifetime instead of fluorescence intensity. This τ-probe exhibited an ultrasensitive response to H(2)S(n), bringing about the lowest value of the detection limit (2 nM) and a lower limit of quantification (10 nM) to date. With such merits, we quantified and mapped endogenous H(2)S(n) within cells and zebrafish. The quantitative information about endogenous H(2)S(n) in cells and in vivo may have a significant implication for future research on the role of H(2)S(n) in biology. The methodology of the τ-probe established here might provide a general insight into the design and application of any fluorescent probes, beyond the limit of utilizing fluorescence intensity. Royal Society of Chemistry 2018-05-29 /pmc/articles/PMC6050607/ /pubmed/30061987 http://dx.doi.org/10.1039/c8sc01879k Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Yang, Fan Gao, He Li, Shan-Shan An, Rui-Bing Sun, Xiao-Yang Kang, Bin Xu, Jing-Juan Chen, Hong-Yuan A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo |
title | A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo
|
title_full | A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo
|
title_fullStr | A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo
|
title_full_unstemmed | A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo
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title_short | A fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo
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title_sort | fluorescent τ-probe: quantitative imaging of ultra-trace endogenous hydrogen polysulfide in cells and in vivo |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050607/ https://www.ncbi.nlm.nih.gov/pubmed/30061987 http://dx.doi.org/10.1039/c8sc01879k |
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