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We are happy to share our recent publication a Protein Language model-based Thermophilicity predictor.

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 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.
Availability and implementation

All code is available in our GitHub repository at


Original Publication (Open Access)
Haselbeck, F., John, M., Zhang, Y., Pirnay, J., Fuenzalida-Werner, J. P., Costa, R. D., & Grimm, D. G. (2023). Superior protein thermophilicity prediction with protein language model embeddings. NAR Genomics and Bioinformatics5(4), lqad087.