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Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy
Super-resolution structured illumination microscopy (SR-SIM) is an optical fluorescence microscopy method which is suitable for imaging a wide variety of cells and tissues in biological and biomedical research. Typically, SIM methods use high spatial frequency illumination patterns generated by lase...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525192/ https://www.ncbi.nlm.nih.gov/pubmed/37760183 http://dx.doi.org/10.3390/bioengineering10091081 |
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author | Paul, Tristan C. Johnson, Karl A. Hagen, Guy M. |
author_facet | Paul, Tristan C. Johnson, Karl A. Hagen, Guy M. |
author_sort | Paul, Tristan C. |
collection | PubMed |
description | Super-resolution structured illumination microscopy (SR-SIM) is an optical fluorescence microscopy method which is suitable for imaging a wide variety of cells and tissues in biological and biomedical research. Typically, SIM methods use high spatial frequency illumination patterns generated by laser interference. This approach provides high resolution but is limited to thin samples such as cultured cells. Using a different strategy for processing raw data and coarser illumination patterns, we imaged through a 150-micrometer-thick coronal section of a mouse brain expressing GFP in a subset of neurons. The resolution reached 144 nm, an improvement of 1.7-fold beyond conventional widefield imaging. |
format | Online Article Text |
id | pubmed-10525192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105251922023-09-28 Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy Paul, Tristan C. Johnson, Karl A. Hagen, Guy M. Bioengineering (Basel) Article Super-resolution structured illumination microscopy (SR-SIM) is an optical fluorescence microscopy method which is suitable for imaging a wide variety of cells and tissues in biological and biomedical research. Typically, SIM methods use high spatial frequency illumination patterns generated by laser interference. This approach provides high resolution but is limited to thin samples such as cultured cells. Using a different strategy for processing raw data and coarser illumination patterns, we imaged through a 150-micrometer-thick coronal section of a mouse brain expressing GFP in a subset of neurons. The resolution reached 144 nm, an improvement of 1.7-fold beyond conventional widefield imaging. MDPI 2023-09-13 /pmc/articles/PMC10525192/ /pubmed/37760183 http://dx.doi.org/10.3390/bioengineering10091081 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Paul, Tristan C. Johnson, Karl A. Hagen, Guy M. Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy |
title | Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy |
title_full | Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy |
title_fullStr | Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy |
title_full_unstemmed | Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy |
title_short | Super-Resolution Imaging of Neuronal Structures with Structured Illumination Microscopy |
title_sort | super-resolution imaging of neuronal structures with structured illumination microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525192/ https://www.ncbi.nlm.nih.gov/pubmed/37760183 http://dx.doi.org/10.3390/bioengineering10091081 |
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