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Topaz-Denoise: general deep denoising models for cryoEM and cryoET
Cryo-electron microscopy (cryoEM) is becoming the preferred method for resolving protein structures. Low signal-to-noise ratio (SNR) in cryoEM images reduces the confidence and throughput of structure determination during several steps of data processing, resulting in impediments such as missing par...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567117/ https://www.ncbi.nlm.nih.gov/pubmed/33060581 http://dx.doi.org/10.1038/s41467-020-18952-1 |
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author | Bepler, Tristan Kelley, Kotaro Noble, Alex J. Berger, Bonnie |
author_facet | Bepler, Tristan Kelley, Kotaro Noble, Alex J. Berger, Bonnie |
author_sort | Bepler, Tristan |
collection | PubMed |
description | Cryo-electron microscopy (cryoEM) is becoming the preferred method for resolving protein structures. Low signal-to-noise ratio (SNR) in cryoEM images reduces the confidence and throughput of structure determination during several steps of data processing, resulting in impediments such as missing particle orientations. Denoising cryoEM images can not only improve downstream analysis but also accelerate the time-consuming data collection process by allowing lower electron dose micrographs to be used for analysis. Here, we present Topaz-Denoise, a deep learning method for reliably and rapidly increasing the SNR of cryoEM images and cryoET tomograms. By training on a dataset composed of thousands of micrographs collected across a wide range of imaging conditions, we are able to learn models capturing the complexity of the cryoEM image formation process. The general model we present is able to denoise new datasets without additional training. Denoising with this model improves micrograph interpretability and allows us to solve 3D single particle structures of clustered protocadherin, an elongated particle with previously elusive views. We then show that low dose collection, enabled by Topaz-Denoise, improves downstream analysis in addition to reducing data collection time. We also present a general 3D denoising model for cryoET. Topaz-Denoise and pre-trained general models are now included in Topaz. We expect that Topaz-Denoise will be of broad utility to the cryoEM community for improving micrograph and tomogram interpretability and accelerating analysis. |
format | Online Article Text |
id | pubmed-7567117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75671172020-10-19 Topaz-Denoise: general deep denoising models for cryoEM and cryoET Bepler, Tristan Kelley, Kotaro Noble, Alex J. Berger, Bonnie Nat Commun Article Cryo-electron microscopy (cryoEM) is becoming the preferred method for resolving protein structures. Low signal-to-noise ratio (SNR) in cryoEM images reduces the confidence and throughput of structure determination during several steps of data processing, resulting in impediments such as missing particle orientations. Denoising cryoEM images can not only improve downstream analysis but also accelerate the time-consuming data collection process by allowing lower electron dose micrographs to be used for analysis. Here, we present Topaz-Denoise, a deep learning method for reliably and rapidly increasing the SNR of cryoEM images and cryoET tomograms. By training on a dataset composed of thousands of micrographs collected across a wide range of imaging conditions, we are able to learn models capturing the complexity of the cryoEM image formation process. The general model we present is able to denoise new datasets without additional training. Denoising with this model improves micrograph interpretability and allows us to solve 3D single particle structures of clustered protocadherin, an elongated particle with previously elusive views. We then show that low dose collection, enabled by Topaz-Denoise, improves downstream analysis in addition to reducing data collection time. We also present a general 3D denoising model for cryoET. Topaz-Denoise and pre-trained general models are now included in Topaz. We expect that Topaz-Denoise will be of broad utility to the cryoEM community for improving micrograph and tomogram interpretability and accelerating analysis. Nature Publishing Group UK 2020-10-15 /pmc/articles/PMC7567117/ /pubmed/33060581 http://dx.doi.org/10.1038/s41467-020-18952-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bepler, Tristan Kelley, Kotaro Noble, Alex J. Berger, Bonnie Topaz-Denoise: general deep denoising models for cryoEM and cryoET |
title | Topaz-Denoise: general deep denoising models for cryoEM and cryoET |
title_full | Topaz-Denoise: general deep denoising models for cryoEM and cryoET |
title_fullStr | Topaz-Denoise: general deep denoising models for cryoEM and cryoET |
title_full_unstemmed | Topaz-Denoise: general deep denoising models for cryoEM and cryoET |
title_short | Topaz-Denoise: general deep denoising models for cryoEM and cryoET |
title_sort | topaz-denoise: general deep denoising models for cryoem and cryoet |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567117/ https://www.ncbi.nlm.nih.gov/pubmed/33060581 http://dx.doi.org/10.1038/s41467-020-18952-1 |
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