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Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain
Hydrogen polysulfides (H(2)S(n)) have a higher number of sulfane sulfur atoms than hydrogen sulfide (H(2)S), which has various physiological roles. We recently found H(2)S(n) in the brain. H(2)S(n) induced some responses previously attributed to H(2)S but with much greater potency than H(2)S. Howeve...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594004/ https://www.ncbi.nlm.nih.gov/pubmed/26437775 http://dx.doi.org/10.1038/srep14774 |
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author | Kimura, Yuka Toyofuku, Yukiko Koike, Shin Shibuya, Norihiro Nagahara, Noriyuki Lefer, David Ogasawara, Yuki Kimura, Hideo |
author_facet | Kimura, Yuka Toyofuku, Yukiko Koike, Shin Shibuya, Norihiro Nagahara, Noriyuki Lefer, David Ogasawara, Yuki Kimura, Hideo |
author_sort | Kimura, Yuka |
collection | PubMed |
description | Hydrogen polysulfides (H(2)S(n)) have a higher number of sulfane sulfur atoms than hydrogen sulfide (H(2)S), which has various physiological roles. We recently found H(2)S(n) in the brain. H(2)S(n) induced some responses previously attributed to H(2)S but with much greater potency than H(2)S. However, the number of sulfur atoms in H(2)S(n) and its producing enzyme were unknown. Here, we detected H(2)S(3) and H(2)S, which were produced from 3-mercaptopyruvate (3 MP) by 3-mercaptopyruvate sulfurtransferase (3MST), in the brain. High performance liquid chromatography with fluorescence detection (LC-FL) and tandem mass spectrometry (LC-MS/MS) analyses showed that H(2)S(3) and H(2)S were produced from 3 MP in the brain cells of wild-type mice but not 3MST knockout (3MST-KO) mice. Purified recombinant 3MST and lysates of COS cells expressing 3MST produced H(2)S(3) from 3 MP, while those expressing defective 3MST mutants did not. H(2)S(3) was localized in the cytosol of cells. H(2)S(3) was also produced from H(2)S by 3MST and rhodanese. H(2)S(2) was identified as a minor H(2)S(n), and 3 MP did not affect the H(2)S(5) level. The present study provides new insights into the physiology of H(2)S(3) and H(2)S, as well as novel therapeutic targets for diseases in which these molecules are involved. |
format | Online Article Text |
id | pubmed-4594004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45940042015-10-13 Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain Kimura, Yuka Toyofuku, Yukiko Koike, Shin Shibuya, Norihiro Nagahara, Noriyuki Lefer, David Ogasawara, Yuki Kimura, Hideo Sci Rep Article Hydrogen polysulfides (H(2)S(n)) have a higher number of sulfane sulfur atoms than hydrogen sulfide (H(2)S), which has various physiological roles. We recently found H(2)S(n) in the brain. H(2)S(n) induced some responses previously attributed to H(2)S but with much greater potency than H(2)S. However, the number of sulfur atoms in H(2)S(n) and its producing enzyme were unknown. Here, we detected H(2)S(3) and H(2)S, which were produced from 3-mercaptopyruvate (3 MP) by 3-mercaptopyruvate sulfurtransferase (3MST), in the brain. High performance liquid chromatography with fluorescence detection (LC-FL) and tandem mass spectrometry (LC-MS/MS) analyses showed that H(2)S(3) and H(2)S were produced from 3 MP in the brain cells of wild-type mice but not 3MST knockout (3MST-KO) mice. Purified recombinant 3MST and lysates of COS cells expressing 3MST produced H(2)S(3) from 3 MP, while those expressing defective 3MST mutants did not. H(2)S(3) was localized in the cytosol of cells. H(2)S(3) was also produced from H(2)S by 3MST and rhodanese. H(2)S(2) was identified as a minor H(2)S(n), and 3 MP did not affect the H(2)S(5) level. The present study provides new insights into the physiology of H(2)S(3) and H(2)S, as well as novel therapeutic targets for diseases in which these molecules are involved. Nature Publishing Group 2015-10-06 /pmc/articles/PMC4594004/ /pubmed/26437775 http://dx.doi.org/10.1038/srep14774 Text en Copyright © 2015, 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 Kimura, Yuka Toyofuku, Yukiko Koike, Shin Shibuya, Norihiro Nagahara, Noriyuki Lefer, David Ogasawara, Yuki Kimura, Hideo Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain |
title | Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain |
title_full | Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain |
title_fullStr | Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain |
title_full_unstemmed | Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain |
title_short | Identification of H(2)S(3) and H(2)S produced by 3-mercaptopyruvate sulfurtransferase in the brain |
title_sort | identification of h(2)s(3) and h(2)s produced by 3-mercaptopyruvate sulfurtransferase in the brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594004/ https://www.ncbi.nlm.nih.gov/pubmed/26437775 http://dx.doi.org/10.1038/srep14774 |
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