Superior protein thermophilicity prediction with protein language model embeddings

Author:

Haselbeck Florian12ORCID,John Maura12,Zhang Yuqi1,Pirnay Jonathan12,Fuenzalida-Werner Juan Pablo3,Costa Rubén D3,Grimm Dominik G124ORCID

Affiliation:

1. Technical University of Munich, Campus Straubing for Biotechnology and Sustainability , Bioinformatics, 94315 Straubing, Germany

2. Weihenstephan-Triesdorf University of Applied Sciences , Bioinformatics, 94315 Straubing, Germany

3. Technical University of Munich, Campus Straubing for Biotechnology and Sustainability , Chair of Biogenic Functional Materials, 94315 Straubing, Germany

4. Technical University of Munich, TUM School of Computation, Information and Technology (CIT) , 85748 Garching, Germany

Abstract

Abstract 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.

Funder

Technical University of Munich

Publisher

Oxford University Press (OUP)

Subject

Applied Mathematics,Computer Science Applications,Genetics,Molecular Biology,Structural Biology

Reference67 articles.

1. Two strategies to engineer flexible loops for improved enzyme thermostability;Yu;Sci. Rep.,2017

2. Review: Engineering of thermostable enzymes for industrial applications;Rigoldi;APL Bioeng.,2018

3. Chapter 5: Enzyme engineering strategies to confer thermostability;Xu,2020

4. When fluorescent proteins meet white light-emitting diodes;Fernández-Luna;Angew. Chem. Int. Ed. Engl.,2018

5. Merging biology and solid-state lighting: recent advances in light-emitting diodes based on biological materials;Fresta;Adv. Funct. Mater.,2018

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