Cargando…

Latent generative landscapes as maps of functional diversity in protein sequence space

Variational autoencoders are unsupervised learning models with generative capabilities, when applied to protein data, they classify sequences by phylogeny and generate de novo sequences which preserve statistical properties of protein composition. While previous studies focus on clustering and gener...

Descripción completa

Detalles Bibliográficos
Autores principales: Ziegler, Cheyenne, Martin, Jonathan, Sinner, Claude, Morcos, Faruck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113739/
https://www.ncbi.nlm.nih.gov/pubmed/37076519
http://dx.doi.org/10.1038/s41467-023-37958-z
_version_ 1785027909413502976
author Ziegler, Cheyenne
Martin, Jonathan
Sinner, Claude
Morcos, Faruck
author_facet Ziegler, Cheyenne
Martin, Jonathan
Sinner, Claude
Morcos, Faruck
author_sort Ziegler, Cheyenne
collection PubMed
description Variational autoencoders are unsupervised learning models with generative capabilities, when applied to protein data, they classify sequences by phylogeny and generate de novo sequences which preserve statistical properties of protein composition. While previous studies focus on clustering and generative features, here, we evaluate the underlying latent manifold in which sequence information is embedded. To investigate properties of the latent manifold, we utilize direct coupling analysis and a Potts Hamiltonian model to construct a latent generative landscape. We showcase how this landscape captures phylogenetic groupings, functional and fitness properties of several systems including Globins, β-lactamases, ion channels, and transcription factors. We provide support on how the landscape helps us understand the effects of sequence variability observed in experimental data and provides insights on directed and natural protein evolution. We propose that combining generative properties and functional predictive power of variational autoencoders and coevolutionary analysis could be beneficial in applications for protein engineering and design.
format Online
Article
Text
id pubmed-10113739
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-101137392023-04-20 Latent generative landscapes as maps of functional diversity in protein sequence space Ziegler, Cheyenne Martin, Jonathan Sinner, Claude Morcos, Faruck Nat Commun Article Variational autoencoders are unsupervised learning models with generative capabilities, when applied to protein data, they classify sequences by phylogeny and generate de novo sequences which preserve statistical properties of protein composition. While previous studies focus on clustering and generative features, here, we evaluate the underlying latent manifold in which sequence information is embedded. To investigate properties of the latent manifold, we utilize direct coupling analysis and a Potts Hamiltonian model to construct a latent generative landscape. We showcase how this landscape captures phylogenetic groupings, functional and fitness properties of several systems including Globins, β-lactamases, ion channels, and transcription factors. We provide support on how the landscape helps us understand the effects of sequence variability observed in experimental data and provides insights on directed and natural protein evolution. We propose that combining generative properties and functional predictive power of variational autoencoders and coevolutionary analysis could be beneficial in applications for protein engineering and design. Nature Publishing Group UK 2023-04-19 /pmc/articles/PMC10113739/ /pubmed/37076519 http://dx.doi.org/10.1038/s41467-023-37958-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ziegler, Cheyenne
Martin, Jonathan
Sinner, Claude
Morcos, Faruck
Latent generative landscapes as maps of functional diversity in protein sequence space
title Latent generative landscapes as maps of functional diversity in protein sequence space
title_full Latent generative landscapes as maps of functional diversity in protein sequence space
title_fullStr Latent generative landscapes as maps of functional diversity in protein sequence space
title_full_unstemmed Latent generative landscapes as maps of functional diversity in protein sequence space
title_short Latent generative landscapes as maps of functional diversity in protein sequence space
title_sort latent generative landscapes as maps of functional diversity in protein sequence space
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113739/
https://www.ncbi.nlm.nih.gov/pubmed/37076519
http://dx.doi.org/10.1038/s41467-023-37958-z
work_keys_str_mv AT zieglercheyenne latentgenerativelandscapesasmapsoffunctionaldiversityinproteinsequencespace
AT martinjonathan latentgenerativelandscapesasmapsoffunctionaldiversityinproteinsequencespace
AT sinnerclaude latentgenerativelandscapesasmapsoffunctionaldiversityinproteinsequencespace
AT morcosfaruck latentgenerativelandscapesasmapsoffunctionaldiversityinproteinsequencespace