利用自监督去噪模型完善冷冻电子显微镜三维图:crefDenoiser。

IF 2.9 2区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
IUCrJ Pub Date : 2024-09-01 DOI:10.1107/S2052252524005918
Ishaant Agarwal , Joanna Kaczmar-Michalska , Simon F. Nørrelykke , Andrzej J. Rzepiela
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引用次数: 0

摘要

低温电子显微镜(cryo-EM)是对大分子结构进行成像的关键技术。然而,尽管对低温电子显微镜实验中收集的大型图像集进行了大量处理以提高信噪比,但由于残留噪声的影响,重建的三维蛋白质密度图的质量往往有限,进而影响了大分子表征的准确性。这里介绍的 crefDenoiser 是一种去噪神经网络模型,旨在增强用标准处理流水线生成的三维冷冻电镜图中的信号。crefDenoiser 模型的训练不需要 "干净 "的地面实况目标图。取而代之的是一个定制数据集,该数据集由来自电子显微镜数据库的真实噪声蛋白质半图组成。crefDenoiser 可与当前最先进的技术相媲美,其设计目的是在自我监督训练过程中优化理论上的无噪声图谱。我们证明,我们的模型成功地放大了各种蛋白质图谱的信号,其性能优于经典的图谱去噪器和基于网络的锐化模型。在不对图谱产生偏差的情况下,所提出的去噪方法提高了蛋白质结构特征的可见度,包括蛋白质结构域、二级结构元素和适度的高分辨率特征恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Refinement of cryo-EM 3D maps with a self-supervised denoising model: crefDenoiser

State-of-the-art 3D cryo-EM map denoising with a self-supervised neural network model optimized for theoretical noise-free maps is introduced.

Cryogenic electron microscopy (cryo-EM) is a pivotal technique for imaging macromolecular structures. However, despite extensive processing of large image sets collected in cryo-EM experiments to amplify the signal-to-noise ratio, the reconstructed 3D protein-density maps are often limited in quality due to residual noise, which in turn affects the accuracy of the macromolecular representation. Here, crefDenoiser is introduced, a denoising neural network model designed to enhance the signal in 3D cryo-EM maps produced with standard processing pipelines. The crefDenoiser model is trained without the need for ‘clean’ ground-truth target maps. Instead, a custom dataset is employed, composed of real noisy protein half-maps sourced from the Electron Microscopy Data Bank repository. Competing with the current state-of-the-art, crefDenoiser is designed to optimize for the theoretical noise-free map during self-supervised training. We demonstrate that our model successfully amplifies the signal across a wide variety of protein maps, outperforming a classic map denoiser and following a network-based sharpening model. Without biasing the map, the proposed denoising method leads to improved visibility of protein structural features, including protein domains, secondary structure elements and modest high-resolution feature restoration.

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来源期刊
IUCrJ
IUCrJ CHEMISTRY, MULTIDISCIPLINARYCRYSTALLOGRAPH-CRYSTALLOGRAPHY
CiteScore
7.50
自引率
5.10%
发文量
95
审稿时长
10 weeks
期刊介绍: IUCrJ is a new fully open-access peer-reviewed journal from the International Union of Crystallography (IUCr). The journal will publish high-profile articles on all aspects of the sciences and technologies supported by the IUCr via its commissions, including emerging fields where structural results underpin the science reported in the article. Our aim is to make IUCrJ the natural home for high-quality structural science results. Chemists, biologists, physicists and material scientists will be actively encouraged to report their structural studies in IUCrJ.
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