CryoDRGN2: Ab initio neural reconstruction of 3D protein structures from real cryo-EM images

Ellen D. Zhong, Adam K. Lerer, Joey Davis, B. Berger
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引用次数: 37

Abstract

Protein structure determination from cryo-EM data requires reconstructing a 3D volume (or distribution of volumes) from many noisy and randomly oriented 2D projection images. While the standard homogeneous reconstruction task aims to recover a single static structure, recently-proposed neural and non-neural methods can reconstruct distributions of structures, thereby enabling the study of protein complexes that possess intrinsic structural or conformational heterogeneity. These heterogeneous reconstruction methods, however, require fixed image poses, which are typically estimated from an upstream homogeneous reconstruction and are not guaranteed to be accurate under highly heterogeneous conditions.In this work we describe cryoDRGN2, an ab initio reconstruction algorithm, which can jointly estimate image poses and learn a neural model of a distribution of 3D structures on real heterogeneous cryo-EM data. To achieve this, we adapt search algorithms from the traditional cryo-EM literature, and describe the optimizations and design choices required to make such a search procedure computationally tractable in the neural model setting. We show that cryoDRGN2 is robust to the high noise levels of real cryo-EM images, trains faster than earlier neural methods, and achieves state-of-the-art performance on real cryo-EM datasets.
CryoDRGN2:基于真实冷冻电镜图像的三维蛋白质结构从头算神经重建
从冷冻电镜数据中确定蛋白质结构需要从许多噪声和随机定向的2D投影图像中重建3D体积(或体积分布)。虽然标准的均质重建任务旨在恢复单个静态结构,但最近提出的神经和非神经方法可以重建结构的分布,从而能够研究具有内在结构或构象异质性的蛋白质复合物。然而,这些异构重建方法需要固定的图像姿态,这些姿态通常是从上游的均匀重建中估计出来的,并且不能保证在高度异构的条件下是准确的。在这项工作中,我们描述了一种从头开始重建算法cryoDRGN2,它可以联合估计图像姿态并学习真实异质低温电镜数据上三维结构分布的神经模型。为了实现这一目标,我们采用了传统低温电镜文献中的搜索算法,并描述了在神经模型设置中使这种搜索过程易于计算的优化和设计选择。我们表明,cryoDRGN2对真实低温电镜图像的高噪声水平具有鲁棒性,比早期的神经方法训练速度更快,并且在真实低温电镜数据集上实现了最先进的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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