Published June 5, 2023 | Version v1
Journal article Open

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

Description

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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alvarado-et-al-2023-denoising-autoencoder-trained-on-simulation-derived-structures-for-noise-reduction-in-chromatin.pdf

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Additional details

Identifiers

DOI
10.1021/acscentsci.3c00178
Other
oai:uchicago.tind.io:13448

Funding

National Science Foundation
EFRI CEE 1830969
National Science Foundation
EFMA-1830961
National Institutes of Health
U54CA268084
National Institutes of Health
R01CA228272
National Institutes of Health
R01CA225002
Rob and Kristin Goldman
National Science Foundation
DMR-1828629
National Science Foundation
ECCS-2025633
National Science Foundation
DMR-1720139

UChicago Information

Division(s)
Biological Sciences Division, Pritzker School of Molecular Engineering
Department(s)
Biophysical Sciences