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Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy
Confocal Raman microspectroscopy was used to study the interaction between pulsed electric fields and live cells from a molecular point of view in a non-invasive and label-free manner. Raman signatures of live human adipose-derived mesenchymal stem cells exposed or not to pulsed electric fields (8 p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244372/ https://www.ncbi.nlm.nih.gov/pubmed/28102326 http://dx.doi.org/10.1038/srep40448 |
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author | Azan, Antoine Untereiner, Valérie Gobinet, Cyril Sockalingum, Ganesh D. Breton, Marie Piot, Olivier Mir, Lluis M. |
author_facet | Azan, Antoine Untereiner, Valérie Gobinet, Cyril Sockalingum, Ganesh D. Breton, Marie Piot, Olivier Mir, Lluis M. |
author_sort | Azan, Antoine |
collection | PubMed |
description | Confocal Raman microspectroscopy was used to study the interaction between pulsed electric fields and live cells from a molecular point of view in a non-invasive and label-free manner. Raman signatures of live human adipose-derived mesenchymal stem cells exposed or not to pulsed electric fields (8 pulses, 1 000 V/cm, 100 μs, 1 Hz) were acquired at two cellular locations (nucleus and cytoplasm) and two spectral bands (600–1 800 cm(−1) and 2 800–3 100 cm(−1)). Vibrational modes of proteins (phenylalanine and amide I) and lipids were found to be modified by the electropermeabilization process with a statistically significant difference. The relative magnitude of four phenylalanine peaks decreased in the spectra of the pulsed group. On the contrary, the relative magnitude of the amide I band at 1658 cm(−1) increased by 40% when comparing pulsed and control group. No difference was found between the control and the pulsed group in the high wavenumber spectral band. Our results reveal the modification of proteins in living cells exposed to pulsed electric fields by means of confocal Raman microspectroscopy. |
format | Online Article Text |
id | pubmed-5244372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52443722017-01-23 Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy Azan, Antoine Untereiner, Valérie Gobinet, Cyril Sockalingum, Ganesh D. Breton, Marie Piot, Olivier Mir, Lluis M. Sci Rep Article Confocal Raman microspectroscopy was used to study the interaction between pulsed electric fields and live cells from a molecular point of view in a non-invasive and label-free manner. Raman signatures of live human adipose-derived mesenchymal stem cells exposed or not to pulsed electric fields (8 pulses, 1 000 V/cm, 100 μs, 1 Hz) were acquired at two cellular locations (nucleus and cytoplasm) and two spectral bands (600–1 800 cm(−1) and 2 800–3 100 cm(−1)). Vibrational modes of proteins (phenylalanine and amide I) and lipids were found to be modified by the electropermeabilization process with a statistically significant difference. The relative magnitude of four phenylalanine peaks decreased in the spectra of the pulsed group. On the contrary, the relative magnitude of the amide I band at 1658 cm(−1) increased by 40% when comparing pulsed and control group. No difference was found between the control and the pulsed group in the high wavenumber spectral band. Our results reveal the modification of proteins in living cells exposed to pulsed electric fields by means of confocal Raman microspectroscopy. Nature Publishing Group 2017-01-19 /pmc/articles/PMC5244372/ /pubmed/28102326 http://dx.doi.org/10.1038/srep40448 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 Azan, Antoine Untereiner, Valérie Gobinet, Cyril Sockalingum, Ganesh D. Breton, Marie Piot, Olivier Mir, Lluis M. Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy |
title | Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy |
title_full | Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy |
title_fullStr | Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy |
title_full_unstemmed | Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy |
title_short | Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy |
title_sort | demonstration of the protein involvement in cell electropermeabilization using confocal raman microspectroscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244372/ https://www.ncbi.nlm.nih.gov/pubmed/28102326 http://dx.doi.org/10.1038/srep40448 |
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