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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
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.
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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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