A convolutional autoencoder approach for mining features in cellular electron cryo-tomograms and weakly supervised coarse segmentation

Publication date

2018-05

Authors

Zeng, Xiangrui
Leung, Miguel RicardoISNI 0000000492906538
Zeev-Ben-Mordehai, TzviyaISNI 0000000492962767
Xu, Min

Editors

Advisors

Supervisors

Document Type

Article
Open Access logo

License

taverne

Abstract

Cellular electron cryo-tomography enables the 3D visualization of cellular organization in the near-native state and at submolecular resolution. However, the contents of cellular tomograms are often complex, making it difficult to automatically isolate different in situ cellular components. In this paper, we propose a convolutional autoencoder-based unsupervised approach to provide a coarse grouping of 3D small subvolumes extracted from tomograms. We demonstrate that the autoencoder can be used for efficient and coarse characterization of features of macromolecular complexes and surfaces, such as membranes. In addition, the autoencoder can be used to detect non-cellular features related to sample preparation and data collection, such as carbon edges from the grid and tomogram boundaries. The autoencoder is also able to detect patterns that may indicate spatial interactions between cellular components. Furthermore, we demonstrate that our autoencoder can be used for weakly supervised semantic segmentation of cellular components, requiring a very small amount of manual annotation.

Keywords

Cellular electron cryo-tomography, Macromolecular complex, Subtomogram classification, Visual proteomics, Particle picking, Structural pattern mining, Deep learning, Convolutional neural network, Convolutional autoencoder, Image semantic segmentation, Machine learning, Unsupervised learning, Weakly supervised learning, Pose normalization, Taverne

Citation

Zeng, X, Leung, M R, Zeev-ben-mordehai, T & Xu, M 2018, 'A convolutional autoencoder approach for mining features in cellular electron cryo-tomograms and weakly supervised coarse segmentation', Journal of Structural Biology, vol. 202, no. 2, pp. 150-160. https://doi.org/10.1016/j.jsb.2017.12.015