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Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm
High-resolution optical microscopes that can break 180 nm in spatial resolution set to conventional microscopies are much-needed tools. However, current optical microscopes have to rely on exogenous fluorescent labels to achieve high resolution in biological imaging. Herein, we report near-resonance...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199294/ https://www.ncbi.nlm.nih.gov/pubmed/30374403 http://dx.doi.org/10.1038/s41377-018-0082-1 |
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author | Bi, Yali Yang, Chi Chen, Yage Yan, Shuai Yang, Guang Wu, Yaozu Zhang, Guoping Wang, Ping |
author_facet | Bi, Yali Yang, Chi Chen, Yage Yan, Shuai Yang, Guang Wu, Yaozu Zhang, Guoping Wang, Ping |
author_sort | Bi, Yali |
collection | PubMed |
description | High-resolution optical microscopes that can break 180 nm in spatial resolution set to conventional microscopies are much-needed tools. However, current optical microscopes have to rely on exogenous fluorescent labels to achieve high resolution in biological imaging. Herein, we report near-resonance enhanced label-free stimulated Raman scattering (SRS) microscopy with a lateral resolution near 130 nm, in which the high-resolution image contrast originates directly from a low concentration of endogenous biomolecules, with sensitivity gains of approximately 23 times. Moreover, by using a 0.3-m-long optical fiber, we developed hyperspectral SRS microscopy based on spectral focusing technology. Attributed to enhancements in spatial resolution and sensitivity, we demonstrated high-resolution imaging of three-dimensional structures in single cells and high-resolution mapping of large-scale intact mouse brain tissues in situ. By using enhanced high-resolution hyperspectral SRS, we chemically observed sphingomyelin distributed in the myelin sheath that insulates single axons. Our concept opens the door to biomedical imaging with ~130 nm resolution. |
format | Online Article Text |
id | pubmed-6199294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61992942018-10-29 Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm Bi, Yali Yang, Chi Chen, Yage Yan, Shuai Yang, Guang Wu, Yaozu Zhang, Guoping Wang, Ping Light Sci Appl Article High-resolution optical microscopes that can break 180 nm in spatial resolution set to conventional microscopies are much-needed tools. However, current optical microscopes have to rely on exogenous fluorescent labels to achieve high resolution in biological imaging. Herein, we report near-resonance enhanced label-free stimulated Raman scattering (SRS) microscopy with a lateral resolution near 130 nm, in which the high-resolution image contrast originates directly from a low concentration of endogenous biomolecules, with sensitivity gains of approximately 23 times. Moreover, by using a 0.3-m-long optical fiber, we developed hyperspectral SRS microscopy based on spectral focusing technology. Attributed to enhancements in spatial resolution and sensitivity, we demonstrated high-resolution imaging of three-dimensional structures in single cells and high-resolution mapping of large-scale intact mouse brain tissues in situ. By using enhanced high-resolution hyperspectral SRS, we chemically observed sphingomyelin distributed in the myelin sheath that insulates single axons. Our concept opens the door to biomedical imaging with ~130 nm resolution. Nature Publishing Group UK 2018-10-24 /pmc/articles/PMC6199294/ /pubmed/30374403 http://dx.doi.org/10.1038/s41377-018-0082-1 Text en © The Author(s) 2018 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 Bi, Yali Yang, Chi Chen, Yage Yan, Shuai Yang, Guang Wu, Yaozu Zhang, Guoping Wang, Ping Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm |
title | Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm |
title_full | Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm |
title_fullStr | Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm |
title_full_unstemmed | Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm |
title_short | Near-resonance enhanced label-free stimulated Raman scattering microscopy with spatial resolution near 130 nm |
title_sort | near-resonance enhanced label-free stimulated raman scattering microscopy with spatial resolution near 130 nm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199294/ https://www.ncbi.nlm.nih.gov/pubmed/30374403 http://dx.doi.org/10.1038/s41377-018-0082-1 |
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