Ig-VAE: Generative modeling of protein structure by direct 3D coordinate generation

61Citations
Citations of this article
75Readers
Mendeley users who have this article in their library.
Get full text

Abstract

While deep learning models have seen increasing applications in protein science, few have been implemented for protein backbone generation—an important task in structure-based problems such as active site and interface design. We present a new approach to building class-specific backbones, using a variational auto-encoder to directly generate the 3D coordinates of immunoglobulins. Our model is torsion- and distance-aware, learns a high-resolution embedding of the dataset, and generates novel, high-quality structures compatible with existing design tools. We show that the Ig-VAE can be used with Rosetta to create a computational model of a SARS-CoV2-RBD binder via latent space sampling. We further demonstrate that the model’s generative prior is a powerful tool for guiding computational protein design, motivating a new paradigm under which backbone design is solved as constrained optimization problem in the latent space of a generative model.

Cite

CITATION STYLE

APA

Eguchi, R. R., Choe, C. A., & Huang, P. S. (2022). Ig-VAE: Generative modeling of protein structure by direct 3D coordinate generation. PLoS Computational Biology, 18(6). https://doi.org/10.1371/journal.pcbi.1010271

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free