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3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning

Cryo-soft X-ray tomography (cryo-SXT) is a powerful method to investigate the ultrastructure of cells, offering resolution in the tens of nanometer range and strong contrast for membranous structures without requiring labeling or chemical fixation. The short acquisition time and the relatively large...

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Autores principales: Dyhr, Michael C. A., Sadeghi, Mohsen, Moynova, Ralitsa, Knappe, Carolin, Kepsutlu Çakmak, Burcu, Werner, Stephan, Schneider, Gerd, McNally, James, Noé, Frank, Ewers, Helge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268598/
https://www.ncbi.nlm.nih.gov/pubmed/37276395
http://dx.doi.org/10.1073/pnas.2209938120
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author Dyhr, Michael C. A.
Sadeghi, Mohsen
Moynova, Ralitsa
Knappe, Carolin
Kepsutlu Çakmak, Burcu
Werner, Stephan
Schneider, Gerd
McNally, James
Noé, Frank
Ewers, Helge
author_facet Dyhr, Michael C. A.
Sadeghi, Mohsen
Moynova, Ralitsa
Knappe, Carolin
Kepsutlu Çakmak, Burcu
Werner, Stephan
Schneider, Gerd
McNally, James
Noé, Frank
Ewers, Helge
author_sort Dyhr, Michael C. A.
collection PubMed
description Cryo-soft X-ray tomography (cryo-SXT) is a powerful method to investigate the ultrastructure of cells, offering resolution in the tens of nanometer range and strong contrast for membranous structures without requiring labeling or chemical fixation. The short acquisition time and the relatively large field of view leads to fast acquisition of large amounts of tomographic image data. Segmentation of these data into accessible features is a necessary step in gaining biologically relevant information from cryo-soft X-ray tomograms. However, manual image segmentation still requires several orders of magnitude more time than data acquisition. To address this challenge, we have here developed an end-to-end automated 3D segmentation pipeline based on semisupervised deep learning. Our approach is suitable for high-throughput analysis of large amounts of tomographic data, while being robust when faced with limited manual annotations and variations in the tomographic conditions. We validate our approach by extracting three-dimensional information on cellular ultrastructure and by quantifying nanoscopic morphological parameters of filopodia in mammalian cells.
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spelling pubmed-102685982023-06-16 3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning Dyhr, Michael C. A. Sadeghi, Mohsen Moynova, Ralitsa Knappe, Carolin Kepsutlu Çakmak, Burcu Werner, Stephan Schneider, Gerd McNally, James Noé, Frank Ewers, Helge Proc Natl Acad Sci U S A Biological Sciences Cryo-soft X-ray tomography (cryo-SXT) is a powerful method to investigate the ultrastructure of cells, offering resolution in the tens of nanometer range and strong contrast for membranous structures without requiring labeling or chemical fixation. The short acquisition time and the relatively large field of view leads to fast acquisition of large amounts of tomographic image data. Segmentation of these data into accessible features is a necessary step in gaining biologically relevant information from cryo-soft X-ray tomograms. However, manual image segmentation still requires several orders of magnitude more time than data acquisition. To address this challenge, we have here developed an end-to-end automated 3D segmentation pipeline based on semisupervised deep learning. Our approach is suitable for high-throughput analysis of large amounts of tomographic data, while being robust when faced with limited manual annotations and variations in the tomographic conditions. We validate our approach by extracting three-dimensional information on cellular ultrastructure and by quantifying nanoscopic morphological parameters of filopodia in mammalian cells. National Academy of Sciences 2023-06-05 2023-06-13 /pmc/articles/PMC10268598/ /pubmed/37276395 http://dx.doi.org/10.1073/pnas.2209938120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Dyhr, Michael C. A.
Sadeghi, Mohsen
Moynova, Ralitsa
Knappe, Carolin
Kepsutlu Çakmak, Burcu
Werner, Stephan
Schneider, Gerd
McNally, James
Noé, Frank
Ewers, Helge
3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning
title 3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning
title_full 3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning
title_fullStr 3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning
title_full_unstemmed 3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning
title_short 3D surface reconstruction of cellular cryo-soft X-ray microscopy tomograms using semisupervised deep learning
title_sort 3d surface reconstruction of cellular cryo-soft x-ray microscopy tomograms using semisupervised deep learning
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268598/
https://www.ncbi.nlm.nih.gov/pubmed/37276395
http://dx.doi.org/10.1073/pnas.2209938120
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