Cargando…
Superior protein thermophilicity prediction with protein language model embeddings
Protein thermostability is important in many areas of biotechnology, including enzyme engineering and protein-hybrid optoelectronics. Ever-growing protein databases and information on stability at different temperatures allow the training of machine learning models to predict whether proteins are th...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566323/ https://www.ncbi.nlm.nih.gov/pubmed/37829176 http://dx.doi.org/10.1093/nargab/lqad087 |
_version_ | 1785118899356827648 |
---|---|
author | Haselbeck, Florian John, Maura Zhang, Yuqi Pirnay, Jonathan Fuenzalida-Werner, Juan Pablo Costa, Rubén D Grimm, Dominik G |
author_facet | Haselbeck, Florian John, Maura Zhang, Yuqi Pirnay, Jonathan Fuenzalida-Werner, Juan Pablo Costa, Rubén D Grimm, Dominik G |
author_sort | Haselbeck, Florian |
collection | PubMed |
description | Protein thermostability is important in many areas of biotechnology, including enzyme engineering and protein-hybrid optoelectronics. Ever-growing protein databases and information on stability at different temperatures allow the training of machine learning models to predict whether proteins are thermophilic. In silico predictions could reduce costs and accelerate the development process by guiding researchers to more promising candidates. Existing models for predicting protein thermophilicity rely mainly on features derived from physicochemical properties. Recently, modern protein language models that directly use sequence information have demonstrated superior performance in several tasks. In this study, we evaluate the usefulness of protein language model embeddings for thermophilicity prediction with ProLaTherm, a Protein Language model-based Thermophilicity predictor. ProLaTherm significantly outperforms all feature-, sequence- and literature-based comparison partners on multiple evaluation metrics. In terms of the Matthew’s correlation coefficient, ProLaTherm outperforms the second-best competitor by 18.1% in a nested cross-validation setup. Using proteins from species not overlapping with species from the training data, ProLaTherm outperforms all competitors by at least 9.7%. On these data, it misclassified only one nonthermophilic protein as thermophilic. Furthermore, it correctly identified 97.4% of all thermophilic proteins in our test set with an optimal growth temperature above 70°C. |
format | Online Article Text |
id | pubmed-10566323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105663232023-10-12 Superior protein thermophilicity prediction with protein language model embeddings Haselbeck, Florian John, Maura Zhang, Yuqi Pirnay, Jonathan Fuenzalida-Werner, Juan Pablo Costa, Rubén D Grimm, Dominik G NAR Genom Bioinform Standard Article Protein thermostability is important in many areas of biotechnology, including enzyme engineering and protein-hybrid optoelectronics. Ever-growing protein databases and information on stability at different temperatures allow the training of machine learning models to predict whether proteins are thermophilic. In silico predictions could reduce costs and accelerate the development process by guiding researchers to more promising candidates. Existing models for predicting protein thermophilicity rely mainly on features derived from physicochemical properties. Recently, modern protein language models that directly use sequence information have demonstrated superior performance in several tasks. In this study, we evaluate the usefulness of protein language model embeddings for thermophilicity prediction with ProLaTherm, a Protein Language model-based Thermophilicity predictor. ProLaTherm significantly outperforms all feature-, sequence- and literature-based comparison partners on multiple evaluation metrics. In terms of the Matthew’s correlation coefficient, ProLaTherm outperforms the second-best competitor by 18.1% in a nested cross-validation setup. Using proteins from species not overlapping with species from the training data, ProLaTherm outperforms all competitors by at least 9.7%. On these data, it misclassified only one nonthermophilic protein as thermophilic. Furthermore, it correctly identified 97.4% of all thermophilic proteins in our test set with an optimal growth temperature above 70°C. Oxford University Press 2023-10-11 /pmc/articles/PMC10566323/ /pubmed/37829176 http://dx.doi.org/10.1093/nargab/lqad087 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Standard Article Haselbeck, Florian John, Maura Zhang, Yuqi Pirnay, Jonathan Fuenzalida-Werner, Juan Pablo Costa, Rubén D Grimm, Dominik G Superior protein thermophilicity prediction with protein language model embeddings |
title | Superior protein thermophilicity prediction with protein language model embeddings |
title_full | Superior protein thermophilicity prediction with protein language model embeddings |
title_fullStr | Superior protein thermophilicity prediction with protein language model embeddings |
title_full_unstemmed | Superior protein thermophilicity prediction with protein language model embeddings |
title_short | Superior protein thermophilicity prediction with protein language model embeddings |
title_sort | superior protein thermophilicity prediction with protein language model embeddings |
topic | Standard Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566323/ https://www.ncbi.nlm.nih.gov/pubmed/37829176 http://dx.doi.org/10.1093/nargab/lqad087 |
work_keys_str_mv | AT haselbeckflorian superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings AT johnmaura superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings AT zhangyuqi superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings AT pirnayjonathan superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings AT fuenzalidawernerjuanpablo superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings AT costarubend superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings AT grimmdominikg superiorproteinthermophilicitypredictionwithproteinlanguagemodelembeddings |