2021Zhong CryoDRGN: Difference between revisions
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== Citation == | == Citation == | ||
Zhong, E. D.; Bepler, T.; Berger, B.; Davis, J. H. CryoDRGN: reconstruction of heterogeneous cryo-EM structures using neural networks. Nature methods, 2021, 18, 176-185 | |||
== Abstract == | == Abstract == |
Latest revision as of 14:33, 1 March 2021
Citation
Zhong, E. D.; Bepler, T.; Berger, B.; Davis, J. H. CryoDRGN: reconstruction of heterogeneous cryo-EM structures using neural networks. Nature methods, 2021, 18, 176-185
Abstract
Cryo-electron microscopy (cryo-EM) single-particle analysis has proven powerful in determining the structures of rigid macromolecules. However, many imaged protein complexes exhibit conformational and compositional heterogeneity that poses a major challenge to existing three-dimensional reconstruction methods. Here, we present cryoDRGN, an algorithm that leverages the representation power of deep neural networks to directly reconstruct continuous distributions of 3D density maps and map per-particle heterogeneity of single-particle cryo-EM datasets. Using cryoDRGN, we uncovered residual heterogeneity in high-resolution datasets of the 80S ribosome and the RAG complex, revealed a new structural state of the assembling 50S ribosome, and visualized large-scale continuous motions of a spliceosome complex. CryoDRGN contains interactive tools to visualize a dataset's distribution of per-particle variability, generate density maps for exploratory analysis, extract particle subsets for use with other tools and generate trajectories to visualize molecular motions. CryoDRGN is open-source software freely available at http://cryodrgn.csail.mit.edu.
Keywords
Links
https://www.nature.com/articles/s41592-020-01049-4