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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...

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Detalles Bibliográficos
Autores principales: Paul, Tristan C., Johnson, Karl A., Hagen, Guy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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