Evidence map›Paper›PMID 39314387›Full record

ArticlebioRxiv : the preprint server for biology2024

CryoTEN: Efficiently Enhancing Cryo-EM Density Maps Using Transformers.

Joel Selvaraj, Liguo Wang, Jianlin Cheng

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Joel SelvarajDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, 65211, MO, United States.ORCID 0000-0003-0068-3262
Liguo WangLaboratory for BioMolecular Structure (LBMS), Brookhaven National Laboratory, Upton, 11973, NY, United States.
Jianlin ChengDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, 65211, MO, United States.ORCID 0000-0003-0305-2853

Funding

Deep learning methods for automated and accurate reconstruction of protein structures from cryo-EM image dataR01GM146340 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHENG, JIANLIN · 2022 to 2025
$1.4M
NIGMS NIH HHS R01 GM146340
6 · The paper itself

Abstract

Motivation: Cryogenic Electron Microscopy (cryo-EM) is a core experimental technique used to determine the structure of macromolecules such as proteins. However, the effectiveness of cryo-EM is often hindered by the noise and missing density values in cryo-EM density maps caused by experimental conditions such as low contrast and conformational heterogeneity. Although various global and local map sharpening techniques are widely employed to improve cryo-EM density maps, it is still challenging to efficiently improve their quality for building better protein structures from them. Results: In this study, we introduce CryoTEN - a three-dimensional U-Net style transformer to improve cryo-EM maps effectively. CryoTEN is trained using a diverse set of 1,295 cryo-EM maps as inputs and their corresponding simulated maps generated from known protein structures as targets. An independent test set containing 150 maps is used to evaluate CryoTEN, and the results demonstrate that it can robustly enhance the quality of cryo-EM density maps. In addition, the automatic de novo protein structure modeling shows that the protein structures built from the density maps processed by CryoTEN have substantially better quality than those built from the original maps. Compared to the existing state-of-the-art deep learning methods for enhancing cryo-EM density maps, CryoTEN ranks second in improving the quality of density maps, while running > 10 times faster and requiring much less GPU memory than them. Availability and implementation: The source code and data is freely available at https://github.com/jianlin-cheng/cryoten.

Indexed as

Cryo-EMDensity Map EnhancementTransformerU-Net

Identifiers

PMID39314387
PMCPMC11418965

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.