Integrating Molecular Models Into CryoEM Heterogeneity Analysis Using Scalable High-resolution Deep Gaussian Mixture Models

被引:12
作者
Chen, Muyuan [1 ]
Toader, Bogdan [2 ]
Lederman, Roy [2 ]
机构
[1] Stanford Univ, Div CryoEM & Bioimaging, SLAC Natl Accelerator Lab, SSRL, Menlo Pk, CA 94305 USA
[2] Yale Univ, Dept Stat & Data Sci, New Haven, CT USA
关键词
CryoEM; single particle analysis; structure heterogeneity; deep neural networks; Gaussian mixture model; VALIDATION; MAPS;
D O I
10.1016/j.jmb.2023.168014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Resolving the structural variability of proteins is often key to understanding the structure-function relationship of those macromolecular machines. Single particle analysis using Cryogenic electron microscopy (CryoEM), combined with machine learning algorithms, provides a way to reveal the dynamics within the protein system from noisy micrographs. Here, we introduce an improved computational method that uses Gaussian mixture models for protein structure representation and deep neural networks for conformation space embedding. By integrating information from molecular models into the heterogeneity analysis, we can analyze continuous protein conformational changes using structural information at the frequency of 1/3 angstrom(-1), and present the results in a more interpretable form. (c) 2023 Elsevier Ltd. All rights reserved.
引用
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页数:12
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