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Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission

Our current understanding of molecular biology provides a clear picture of how the genome, transcriptome and proteome regulate each other, but how the chemical environment of the cell plays a role in cellular regulation remains much to be studied. Here we show an imaging method using hybrid fluoresc...

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Autores principales: Chiu, Liang-da, Ichimura, Taro, Sekiya, Takumasa, Machiyama, Hiroaki, Watanabe, Tomonobu, Fujita, Hideaki, Ozawa, Takeaki, Fujita, Katsumasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341087/
https://www.ncbi.nlm.nih.gov/pubmed/28272392
http://dx.doi.org/10.1038/srep43569
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author Chiu, Liang-da
Ichimura, Taro
Sekiya, Takumasa
Machiyama, Hiroaki
Watanabe, Tomonobu
Fujita, Hideaki
Ozawa, Takeaki
Fujita, Katsumasa
author_facet Chiu, Liang-da
Ichimura, Taro
Sekiya, Takumasa
Machiyama, Hiroaki
Watanabe, Tomonobu
Fujita, Hideaki
Ozawa, Takeaki
Fujita, Katsumasa
author_sort Chiu, Liang-da
collection PubMed
description Our current understanding of molecular biology provides a clear picture of how the genome, transcriptome and proteome regulate each other, but how the chemical environment of the cell plays a role in cellular regulation remains much to be studied. Here we show an imaging method using hybrid fluorescence-Raman microscopy that measures the chemical micro-environment associated with protein expression patterns in a living cell. Simultaneous detection of fluorescence and Raman signals, realised by spectrally separating the two modes through the single photon anti-Stokes fluorescence emission of fluorescent proteins, enables the accurate correlation of the chemical fingerprint of a specimen to its physiological state. Subsequent experiments revealed the slight chemical differences that enabled the chemical profiling of mouse embryonic stem cells with and without Oct4 expression. Furthermore, using the fluorescent probe as localisation guide, we successfully analysed the detailed chemical content of cell nucleus and Golgi body. The technique can be further applied to a wide range of biomedical studies for the better understanding of chemical events during biological processes.
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spelling pubmed-53410872017-03-10 Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission Chiu, Liang-da Ichimura, Taro Sekiya, Takumasa Machiyama, Hiroaki Watanabe, Tomonobu Fujita, Hideaki Ozawa, Takeaki Fujita, Katsumasa Sci Rep Article Our current understanding of molecular biology provides a clear picture of how the genome, transcriptome and proteome regulate each other, but how the chemical environment of the cell plays a role in cellular regulation remains much to be studied. Here we show an imaging method using hybrid fluorescence-Raman microscopy that measures the chemical micro-environment associated with protein expression patterns in a living cell. Simultaneous detection of fluorescence and Raman signals, realised by spectrally separating the two modes through the single photon anti-Stokes fluorescence emission of fluorescent proteins, enables the accurate correlation of the chemical fingerprint of a specimen to its physiological state. Subsequent experiments revealed the slight chemical differences that enabled the chemical profiling of mouse embryonic stem cells with and without Oct4 expression. Furthermore, using the fluorescent probe as localisation guide, we successfully analysed the detailed chemical content of cell nucleus and Golgi body. The technique can be further applied to a wide range of biomedical studies for the better understanding of chemical events during biological processes. Nature Publishing Group 2017-03-08 /pmc/articles/PMC5341087/ /pubmed/28272392 http://dx.doi.org/10.1038/srep43569 Text en Copyright © 2017, The Author(s) 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
Chiu, Liang-da
Ichimura, Taro
Sekiya, Takumasa
Machiyama, Hiroaki
Watanabe, Tomonobu
Fujita, Hideaki
Ozawa, Takeaki
Fujita, Katsumasa
Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission
title Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission
title_full Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission
title_fullStr Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission
title_full_unstemmed Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission
title_short Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission
title_sort protein expression guided chemical profiling of living cells by the simultaneous observation of raman scattering and anti-stokes fluorescence emission
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341087/
https://www.ncbi.nlm.nih.gov/pubmed/28272392
http://dx.doi.org/10.1038/srep43569
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