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3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution
Understanding cellular organization demands the best possible spatial resolution in all three dimensions (3D). In fluorescence microscopy, this is achieved by 4Pi nanoscopy methods that combine the concepts of using two opposing objectives for optimal diffraction-limited 3D resolution with switching...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610943/ https://www.ncbi.nlm.nih.gov/pubmed/34059828 http://dx.doi.org/10.1038/s41592-021-01149-9 |
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author | Hao, Xiang Allgeyer, Edward S. Lee, Dong-Ryoung Antonello, Jacopo Watters, Katherine Gerdes, Julianne A. Schroeder, Lena K. Bottanelli, Francesca Zhao, Jiaxi Kidd, Phylicia Lessard, Mark D. Rothman, James E. Cooley, Lynn Biederer, Thomas Booth, Martin J. Bewersdorf, Joerg |
author_facet | Hao, Xiang Allgeyer, Edward S. Lee, Dong-Ryoung Antonello, Jacopo Watters, Katherine Gerdes, Julianne A. Schroeder, Lena K. Bottanelli, Francesca Zhao, Jiaxi Kidd, Phylicia Lessard, Mark D. Rothman, James E. Cooley, Lynn Biederer, Thomas Booth, Martin J. Bewersdorf, Joerg |
author_sort | Hao, Xiang |
collection | PubMed |
description | Understanding cellular organization demands the best possible spatial resolution in all three dimensions (3D). In fluorescence microscopy, this is achieved by 4Pi nanoscopy methods that combine the concepts of using two opposing objectives for optimal diffraction-limited 3D resolution with switching fluorescent molecules between bright and dark states to break the diffraction limit. However, optical aberrations have limited these nanoscopes to thin samples and prevented their application in thick specimens. Here we have developed an improved isoSTED nanoscope, which utilizes an advanced adaptive optics strategy to achieve sub-50 nm isotropic resolution of structures such as neuronal synapses and ring canals previously inaccessible in tissue. The adaptive optics scheme presented in this work is generally applicable to any microscope with a similar beam path geometry involving two opposing objectives to optimize resolution when imaging deep in aberrating specimens. |
format | Online Article Text |
id | pubmed-7610943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76109432021-11-30 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution Hao, Xiang Allgeyer, Edward S. Lee, Dong-Ryoung Antonello, Jacopo Watters, Katherine Gerdes, Julianne A. Schroeder, Lena K. Bottanelli, Francesca Zhao, Jiaxi Kidd, Phylicia Lessard, Mark D. Rothman, James E. Cooley, Lynn Biederer, Thomas Booth, Martin J. Bewersdorf, Joerg Nat Methods Article Understanding cellular organization demands the best possible spatial resolution in all three dimensions (3D). In fluorescence microscopy, this is achieved by 4Pi nanoscopy methods that combine the concepts of using two opposing objectives for optimal diffraction-limited 3D resolution with switching fluorescent molecules between bright and dark states to break the diffraction limit. However, optical aberrations have limited these nanoscopes to thin samples and prevented their application in thick specimens. Here we have developed an improved isoSTED nanoscope, which utilizes an advanced adaptive optics strategy to achieve sub-50 nm isotropic resolution of structures such as neuronal synapses and ring canals previously inaccessible in tissue. The adaptive optics scheme presented in this work is generally applicable to any microscope with a similar beam path geometry involving two opposing objectives to optimize resolution when imaging deep in aberrating specimens. 2021-06-01 2021-05-31 /pmc/articles/PMC7610943/ /pubmed/34059828 http://dx.doi.org/10.1038/s41592-021-01149-9 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Hao, Xiang Allgeyer, Edward S. Lee, Dong-Ryoung Antonello, Jacopo Watters, Katherine Gerdes, Julianne A. Schroeder, Lena K. Bottanelli, Francesca Zhao, Jiaxi Kidd, Phylicia Lessard, Mark D. Rothman, James E. Cooley, Lynn Biederer, Thomas Booth, Martin J. Bewersdorf, Joerg 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution |
title | 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution |
title_full | 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution |
title_fullStr | 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution |
title_full_unstemmed | 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution |
title_short | 3D Adaptive Optical Nanoscopy for Thick Specimen Imaging at sub-50 nm Resolution |
title_sort | 3d adaptive optical nanoscopy for thick specimen imaging at sub-50 nm resolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610943/ https://www.ncbi.nlm.nih.gov/pubmed/34059828 http://dx.doi.org/10.1038/s41592-021-01149-9 |
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