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Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy

[Image: see text] Scanning transmission electron microscopy tomography with ChromEM staining (ChromSTEM), has allowed for the three-dimensional study of genome organization. By leveraging convolutional neural networks and molecular dynamics simulations, we have developed a denoising autoencoder (DAE...

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Autores principales: Alvarado, Walter, Agrawal, Vasundhara, Li, Wing Shun, Dravid, Vinayak P., Backman, Vadim, de Pablo, Juan J., Ferguson, Andrew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311656/
https://www.ncbi.nlm.nih.gov/pubmed/37396862
http://dx.doi.org/10.1021/acscentsci.3c00178
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author Alvarado, Walter
Agrawal, Vasundhara
Li, Wing Shun
Dravid, Vinayak P.
Backman, Vadim
de Pablo, Juan J.
Ferguson, Andrew L.
author_facet Alvarado, Walter
Agrawal, Vasundhara
Li, Wing Shun
Dravid, Vinayak P.
Backman, Vadim
de Pablo, Juan J.
Ferguson, Andrew L.
author_sort Alvarado, Walter
collection PubMed
description [Image: see text] Scanning transmission electron microscopy tomography with ChromEM staining (ChromSTEM), has allowed for the three-dimensional study of genome organization. By leveraging convolutional neural networks and molecular dynamics simulations, we have developed a denoising autoencoder (DAE) capable of postprocessing experimental ChromSTEM images to provide nucleosome-level resolution. Our DAE is trained on synthetic images generated from simulations of the chromatin fiber using the 1-cylinder per nucleosome (1CPN) model of chromatin. We find that our DAE is capable of removing noise commonly found in high-angle annular dark field (HAADF) STEM experiments and is able to learn structural features driven by the physics of chromatin folding. The DAE outperforms other well-known denoising algorithms without degradation of structural features and permits the resolution of α-tetrahedron tetranucleosome motifs that induce local chromatin compaction and mediate DNA accessibility. Notably, we find no evidence for the 30 nm fiber, which has been suggested to serve as the higher-order structure of the chromatin fiber. This approach provides high-resolution STEM images that allow for the resolution of single nucleosomes and organized domains within chromatin dense regions comprising of folding motifs that modulate the accessibility of DNA to external biological machinery.
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spelling pubmed-103116562023-07-01 Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy Alvarado, Walter Agrawal, Vasundhara Li, Wing Shun Dravid, Vinayak P. Backman, Vadim de Pablo, Juan J. Ferguson, Andrew L. ACS Cent Sci [Image: see text] Scanning transmission electron microscopy tomography with ChromEM staining (ChromSTEM), has allowed for the three-dimensional study of genome organization. By leveraging convolutional neural networks and molecular dynamics simulations, we have developed a denoising autoencoder (DAE) capable of postprocessing experimental ChromSTEM images to provide nucleosome-level resolution. Our DAE is trained on synthetic images generated from simulations of the chromatin fiber using the 1-cylinder per nucleosome (1CPN) model of chromatin. We find that our DAE is capable of removing noise commonly found in high-angle annular dark field (HAADF) STEM experiments and is able to learn structural features driven by the physics of chromatin folding. The DAE outperforms other well-known denoising algorithms without degradation of structural features and permits the resolution of α-tetrahedron tetranucleosome motifs that induce local chromatin compaction and mediate DNA accessibility. Notably, we find no evidence for the 30 nm fiber, which has been suggested to serve as the higher-order structure of the chromatin fiber. This approach provides high-resolution STEM images that allow for the resolution of single nucleosomes and organized domains within chromatin dense regions comprising of folding motifs that modulate the accessibility of DNA to external biological machinery. American Chemical Society 2023-06-05 /pmc/articles/PMC10311656/ /pubmed/37396862 http://dx.doi.org/10.1021/acscentsci.3c00178 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Alvarado, Walter
Agrawal, Vasundhara
Li, Wing Shun
Dravid, Vinayak P.
Backman, Vadim
de Pablo, Juan J.
Ferguson, Andrew L.
Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy
title Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy
title_full Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy
title_fullStr Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy
title_full_unstemmed Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy
title_short Denoising Autoencoder Trained on Simulation-Derived Structures for Noise Reduction in Chromatin Scanning Transmission Electron Microscopy
title_sort denoising autoencoder trained on simulation-derived structures for noise reduction in chromatin scanning transmission electron microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311656/
https://www.ncbi.nlm.nih.gov/pubmed/37396862
http://dx.doi.org/10.1021/acscentsci.3c00178
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