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Super-resolution vibrational microscopy by stimulated Raman excited fluorescence

Inspired by the revolutionary impact of super-resolution fluorescence microscopy, super-resolution Raman imaging has been long pursued because of its much higher chemical specificity than the fluorescence counterpart. However, vibrational contrasts are intrinsically less sensitive compared with fluo...

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Autores principales: Xiong, Hanqing, Qian, Naixin, Miao, Yupeng, Zhao, Zhilun, Chen, Chen, Min, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058038/
https://www.ncbi.nlm.nih.gov/pubmed/33879766
http://dx.doi.org/10.1038/s41377-021-00518-5
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author Xiong, Hanqing
Qian, Naixin
Miao, Yupeng
Zhao, Zhilun
Chen, Chen
Min, Wei
author_facet Xiong, Hanqing
Qian, Naixin
Miao, Yupeng
Zhao, Zhilun
Chen, Chen
Min, Wei
author_sort Xiong, Hanqing
collection PubMed
description Inspired by the revolutionary impact of super-resolution fluorescence microscopy, super-resolution Raman imaging has been long pursued because of its much higher chemical specificity than the fluorescence counterpart. However, vibrational contrasts are intrinsically less sensitive compared with fluorescence, resulting in only mild resolution enhancement beyond the diffraction limit even with strong laser excitation power. As such, it is still a great challenge to achieve biocompatible super-resolution vibrational imaging in the optical far-field. In 2019 Stimulated Raman Excited Fluorescence (SREF) was discovered as an ultrasensitive vibrational spectroscopy that combines the high chemical specificity of Raman scattering and the superb sensitivity of fluorescence detection. Herein we developed a novel super-resolution vibrational imaging method by harnessing SREF as the contrast mechanism. We first identified the undesired role of anti-Stokes fluorescence background in preventing direct adoption of super-resolution fluorescence technique. We then devised a frequency-modulation (FM) strategy to remove the broadband backgrounds and achieved high-contrast SREF imaging. Assisted by newly synthesized SREF dyes, we realized multicolor FM-SREF imaging with nanometer spectral resolution. Finally, by integrating stimulated emission depletion (STED) with background-free FM-SREF, we accomplished high-contrast super-resolution vibrational imaging with STED-FM-SREF whose spatial resolution is only determined by the signal-to-noise ratio. In our proof-of-principle demonstration, more than two times of resolution improvement is achieved in biological systems with moderate laser excitation power, which shall be further refined with optimized instrumentation and imaging probes. With its super resolution, high sensitivity, vibrational contrast, and mild laser excitation power, STED-FM-SREF microscopy is envisioned to aid a wide variety of applications.
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spelling pubmed-80580382021-05-05 Super-resolution vibrational microscopy by stimulated Raman excited fluorescence Xiong, Hanqing Qian, Naixin Miao, Yupeng Zhao, Zhilun Chen, Chen Min, Wei Light Sci Appl Article Inspired by the revolutionary impact of super-resolution fluorescence microscopy, super-resolution Raman imaging has been long pursued because of its much higher chemical specificity than the fluorescence counterpart. However, vibrational contrasts are intrinsically less sensitive compared with fluorescence, resulting in only mild resolution enhancement beyond the diffraction limit even with strong laser excitation power. As such, it is still a great challenge to achieve biocompatible super-resolution vibrational imaging in the optical far-field. In 2019 Stimulated Raman Excited Fluorescence (SREF) was discovered as an ultrasensitive vibrational spectroscopy that combines the high chemical specificity of Raman scattering and the superb sensitivity of fluorescence detection. Herein we developed a novel super-resolution vibrational imaging method by harnessing SREF as the contrast mechanism. We first identified the undesired role of anti-Stokes fluorescence background in preventing direct adoption of super-resolution fluorescence technique. We then devised a frequency-modulation (FM) strategy to remove the broadband backgrounds and achieved high-contrast SREF imaging. Assisted by newly synthesized SREF dyes, we realized multicolor FM-SREF imaging with nanometer spectral resolution. Finally, by integrating stimulated emission depletion (STED) with background-free FM-SREF, we accomplished high-contrast super-resolution vibrational imaging with STED-FM-SREF whose spatial resolution is only determined by the signal-to-noise ratio. In our proof-of-principle demonstration, more than two times of resolution improvement is achieved in biological systems with moderate laser excitation power, which shall be further refined with optimized instrumentation and imaging probes. With its super resolution, high sensitivity, vibrational contrast, and mild laser excitation power, STED-FM-SREF microscopy is envisioned to aid a wide variety of applications. Nature Publishing Group UK 2021-04-20 /pmc/articles/PMC8058038/ /pubmed/33879766 http://dx.doi.org/10.1038/s41377-021-00518-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xiong, Hanqing
Qian, Naixin
Miao, Yupeng
Zhao, Zhilun
Chen, Chen
Min, Wei
Super-resolution vibrational microscopy by stimulated Raman excited fluorescence
title Super-resolution vibrational microscopy by stimulated Raman excited fluorescence
title_full Super-resolution vibrational microscopy by stimulated Raman excited fluorescence
title_fullStr Super-resolution vibrational microscopy by stimulated Raman excited fluorescence
title_full_unstemmed Super-resolution vibrational microscopy by stimulated Raman excited fluorescence
title_short Super-resolution vibrational microscopy by stimulated Raman excited fluorescence
title_sort super-resolution vibrational microscopy by stimulated raman excited fluorescence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058038/
https://www.ncbi.nlm.nih.gov/pubmed/33879766
http://dx.doi.org/10.1038/s41377-021-00518-5
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