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The substrate matters in the Raman spectroscopy analysis of cells
Raman spectroscopy is a powerful analytical method that allows deposited and/or immobilized cells to be evaluated without complex sample preparation or labeling. However, a main limitation of Raman spectroscopy in cell analysis is the extremely weak Raman intensity that results in low signal to nois...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550836/ https://www.ncbi.nlm.nih.gov/pubmed/26310910 http://dx.doi.org/10.1038/srep13150 |
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author | Mikoliunaite, Lina Rodriguez, Raul D. Sheremet, Evgeniya Kolchuzhin, Vladimir Mehner, Jan Ramanavicius, Arunas Zahn, Dietrich R.T. |
author_facet | Mikoliunaite, Lina Rodriguez, Raul D. Sheremet, Evgeniya Kolchuzhin, Vladimir Mehner, Jan Ramanavicius, Arunas Zahn, Dietrich R.T. |
author_sort | Mikoliunaite, Lina |
collection | PubMed |
description | Raman spectroscopy is a powerful analytical method that allows deposited and/or immobilized cells to be evaluated without complex sample preparation or labeling. However, a main limitation of Raman spectroscopy in cell analysis is the extremely weak Raman intensity that results in low signal to noise ratios. Therefore, it is important to seize any opportunity that increases the intensity of the Raman signal and to understand whether and how the signal enhancement changes with respect to the substrate used. Our experimental results show clear differences in the spectroscopic response from cells on different surfaces. This result is partly due to the difference in spatial distribution of electric field at the substrate/cell interface as shown by numerical simulations. We found that the substrate also changes the spatial location of maximum field enhancement around the cells. Moreover, beyond conventional flat surfaces, we introduce an efficient nanostructured silver substrate that largely enhances the Raman signal intensity from a single yeast cell. This work contributes to the field of vibrational spectroscopy analysis by providing a fresh look at the significance of the substrate for Raman investigations in cell research. |
format | Online Article Text |
id | pubmed-4550836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45508362015-09-04 The substrate matters in the Raman spectroscopy analysis of cells Mikoliunaite, Lina Rodriguez, Raul D. Sheremet, Evgeniya Kolchuzhin, Vladimir Mehner, Jan Ramanavicius, Arunas Zahn, Dietrich R.T. Sci Rep Article Raman spectroscopy is a powerful analytical method that allows deposited and/or immobilized cells to be evaluated without complex sample preparation or labeling. However, a main limitation of Raman spectroscopy in cell analysis is the extremely weak Raman intensity that results in low signal to noise ratios. Therefore, it is important to seize any opportunity that increases the intensity of the Raman signal and to understand whether and how the signal enhancement changes with respect to the substrate used. Our experimental results show clear differences in the spectroscopic response from cells on different surfaces. This result is partly due to the difference in spatial distribution of electric field at the substrate/cell interface as shown by numerical simulations. We found that the substrate also changes the spatial location of maximum field enhancement around the cells. Moreover, beyond conventional flat surfaces, we introduce an efficient nanostructured silver substrate that largely enhances the Raman signal intensity from a single yeast cell. This work contributes to the field of vibrational spectroscopy analysis by providing a fresh look at the significance of the substrate for Raman investigations in cell research. Nature Publishing Group 2015-08-27 /pmc/articles/PMC4550836/ /pubmed/26310910 http://dx.doi.org/10.1038/srep13150 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 Mikoliunaite, Lina Rodriguez, Raul D. Sheremet, Evgeniya Kolchuzhin, Vladimir Mehner, Jan Ramanavicius, Arunas Zahn, Dietrich R.T. The substrate matters in the Raman spectroscopy analysis of cells |
title | The substrate matters in the Raman spectroscopy analysis of cells |
title_full | The substrate matters in the Raman spectroscopy analysis of cells |
title_fullStr | The substrate matters in the Raman spectroscopy analysis of cells |
title_full_unstemmed | The substrate matters in the Raman spectroscopy analysis of cells |
title_short | The substrate matters in the Raman spectroscopy analysis of cells |
title_sort | substrate matters in the raman spectroscopy analysis of cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550836/ https://www.ncbi.nlm.nih.gov/pubmed/26310910 http://dx.doi.org/10.1038/srep13150 |
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