Supervised Learning of Protein Melting Temperature: Cross‐Species vs. Species‐Specific Prediction

Protein melting temperatures are important proxies for stability, and frequently probed in protein engineering campaigns, for instance for enzyme discovery and protein optimization. With the emergence of large datasets of melting temperatures for diverse natural proteins, it has become possible to train models to predict this quantity, and the literature has reported impressive performance values in terms of Spearman rho. The high correlation scores suggest that it should be possible to accurately predict melting temperature changes in engineered variants, and to reliably identify naturally thermostable proteins. However, in practice, results in these settings are often disappointing. In this paper, we explore this apparent discrepancy. We show that Spearman rho over cross-species data gives an overly optimistic impression of prediction performance, and that this metric reflects the ability to distinguish global differences in amino acid composition between species, rather than the specific effects of genetic variation. We proceed by investigating whether cross-species training on melting temperature is beneficial at all, compared to training specific models for each species. We address this question using four different transfer-learning approaches and a fine-tuning procedure. Surprisingly, we consistently find no benefit of cross-species training. We conclude that (1) current models for supervised prediction of melting temperature perform substantially worse than the literature suggests, and (2) that reliable transfer across species is still a challenging problem. An implementation of this work is available at https://github.com/deltadedirac/thermocontrast_tm.

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Publication Details

Journal
Proteins Structure Function and Bioinformatics
Published
2025-07-14
DOI
https://doi.org/10.1002/prot.70019
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Supervised Learning of Protein Melting Temperature: Cross‐Species vs. Species‐Specific Prediction

Jesper Salomon, Wouter Boomsma, Secundino López
Proteins Structure Function and Bioinformatics
Protein Structure and Dynamics
article

Supervised Learning of Protein Melting Temperature: Cross‐Species vs. Species‐Specific Prediction

Jesper Salomon, Wouter Boomsma, Secundino López
article en

Abstract

Protein melting temperatures are important proxies for stability, and frequently probed in protein engineering campaigns, for instance for enzyme discovery and protein optimization. With the emergence of large datasets of melting temperatures for diverse natural proteins, it has become possible to train models to predict this quantity, and the literature has reported impressive performance values in terms of Spearman rho. The high correlation scores suggest that it should be possible to accurately predict melting temperature changes in engineered variants, and to reliably identify naturally thermostable proteins. However, in practice, results in these settings are often disappointing. In this paper, we explore this apparent discrepancy. We show that Spearman rho over cross-species data gives an overly optimistic impression of prediction performance, and that this metric reflects the ability to distinguish global differences in amino acid composition between species, rather than the specific effects of genetic variation. We proceed by investigating whether cross-species training on melting temperature is beneficial at all, compared to training specific models for each species. We address this question using four different transfer-learning approaches and a fine-tuning procedure. Surprisingly, we consistently find no benefit of cross-species training. We conclude that (1) current models for supervised prediction of melting temperature perform substantially worse than the literature suggests, and (2) that reliable transfer across species is still a challenging problem. An implementation of this work is available at https://github.com/deltadedirac/thermocontrast_tm.

Proteins Structure Function and BioinformaticsVol. 93(12)
Novozymes (Denmark) (DK), University of Copenhagen (DK), IT University of Copenhagen (DK)
European Commission, Danmarks Grundforskningsfond, Novo Nordisk, Novo Nordisk Fonden, Horizon 2020 Framework Programme, H2020 Marie Skłodowska-Curie Actions
Life in Land
Openalex Percentile: Top 85%
Protein Structure and Dynamics
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