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Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates
Plasmonic hotspots generate a blinking Surface Enhanced Raman Spectroscopy (SERS) effect that can be processed using Stochastic Optical Reconstruction Microscopy (STORM) algorithms for super-resolved imaging. Furthermore, by imaging through a diffraction grating, STORM algorithms can be modified to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567233/ https://www.ncbi.nlm.nih.gov/pubmed/28831104 http://dx.doi.org/10.1038/s41598-017-08915-w |
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author | Olson, Aeli P. Spies, Kelsey B. Browning, Anna C. Soneral, Paula A. G. Lindquist, Nathan C. |
author_facet | Olson, Aeli P. Spies, Kelsey B. Browning, Anna C. Soneral, Paula A. G. Lindquist, Nathan C. |
author_sort | Olson, Aeli P. |
collection | PubMed |
description | Plasmonic hotspots generate a blinking Surface Enhanced Raman Spectroscopy (SERS) effect that can be processed using Stochastic Optical Reconstruction Microscopy (STORM) algorithms for super-resolved imaging. Furthermore, by imaging through a diffraction grating, STORM algorithms can be modified to extract a full SERS spectrum, thereby capturing spectral as well as spatial content simultaneously. Here we demonstrate SERS and STORM combined in this way for super-resolved chemical imaging using an ultra-thin silver substrate. Images of gram-positive and gram-negative bacteria taken with this technique show excellent agreement with scanning electron microscope images, high spatial resolution at <50 nm, and spectral SERS content that can be correlated to different regions. This may be used to identify unique chemical signatures of various cells. Finally, because we image through as-deposited, ultra-thin silver films, this technique requires no nanofabrication beyond a single deposition and looks at the cell samples from below. This allows direct imaging of the cell/substrate interface of thick specimens or imaging samples in turbid or opaque liquids since the optical path doesn’t pass through the sample. These results show promise that super-resolution chemical imaging may be used to differentiate chemical signatures from cells and could be applied to other biological structures of interest. |
format | Online Article Text |
id | pubmed-5567233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55672332017-09-01 Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates Olson, Aeli P. Spies, Kelsey B. Browning, Anna C. Soneral, Paula A. G. Lindquist, Nathan C. Sci Rep Article Plasmonic hotspots generate a blinking Surface Enhanced Raman Spectroscopy (SERS) effect that can be processed using Stochastic Optical Reconstruction Microscopy (STORM) algorithms for super-resolved imaging. Furthermore, by imaging through a diffraction grating, STORM algorithms can be modified to extract a full SERS spectrum, thereby capturing spectral as well as spatial content simultaneously. Here we demonstrate SERS and STORM combined in this way for super-resolved chemical imaging using an ultra-thin silver substrate. Images of gram-positive and gram-negative bacteria taken with this technique show excellent agreement with scanning electron microscope images, high spatial resolution at <50 nm, and spectral SERS content that can be correlated to different regions. This may be used to identify unique chemical signatures of various cells. Finally, because we image through as-deposited, ultra-thin silver films, this technique requires no nanofabrication beyond a single deposition and looks at the cell samples from below. This allows direct imaging of the cell/substrate interface of thick specimens or imaging samples in turbid or opaque liquids since the optical path doesn’t pass through the sample. These results show promise that super-resolution chemical imaging may be used to differentiate chemical signatures from cells and could be applied to other biological structures of interest. Nature Publishing Group UK 2017-08-22 /pmc/articles/PMC5567233/ /pubmed/28831104 http://dx.doi.org/10.1038/s41598-017-08915-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Olson, Aeli P. Spies, Kelsey B. Browning, Anna C. Soneral, Paula A. G. Lindquist, Nathan C. Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates |
title | Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates |
title_full | Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates |
title_fullStr | Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates |
title_full_unstemmed | Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates |
title_short | Chemically imaging bacteria with super-resolution SERS on ultra-thin silver substrates |
title_sort | chemically imaging bacteria with super-resolution sers on ultra-thin silver substrates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567233/ https://www.ncbi.nlm.nih.gov/pubmed/28831104 http://dx.doi.org/10.1038/s41598-017-08915-w |
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