Neural network conditioned to produce thermophilic protein sequences can increase thermal stability

This work presents Neural Optimization for Melting-temperature Enabled by Leveraging Translation (NOMELT), a novel approach for designing and ranking high-temperature stable proteins using neural machine translation. The model, trained on over 4 million protein homologous pairs from organisms adapted to different temperatures, demonstrates promising capability in targeting thermal stability. A designed variant of the Drosophila melanogaster Engrailed Homeodomain shows a melting temperature increase of 15.5 K. Furthermore, NOMELT achieves zero-shot predictive capabilities in ranking experimental melting and half-activation temperatures across a number of protein families. It achieves this without requiring extensive homology data or massive training datasets as do existing zero-shot predictors by specifically learning thermophilicity, as opposed to all natural variation. These findings underscore the potential of leveraging organismal growth temperatures in context-dependent design of proteins for enhanced thermal stability.

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Publication Details

Journal
Scientific Reports
Published
2025-04-23
DOI
https://doi.org/10.1038/s41598-025-90828-0
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Neural network conditioned to produce thermophilic protein sequences can increase thermal stability

Evan Komp, Michelle E. McCully, David A. C. Beck, Humood N. Alanzi et al.
Scientific Reports
Protein Structure and Dynamics
article

Neural network conditioned to produce thermophilic protein sequences can increase thermal stability

Evan Komp, Michelle E. McCully, David A. C. Beck, Humood N. Alanzi, Christian Phillips, Marlo Zorman, Lauren Lee, Shayna M Fallin
article en

Abstract

This work presents Neural Optimization for Melting-temperature Enabled by Leveraging Translation (NOMELT), a novel approach for designing and ranking high-temperature stable proteins using neural machine translation. The model, trained on over 4 million protein homologous pairs from organisms adapted to different temperatures, demonstrates promising capability in targeting thermal stability. A designed variant of the Drosophila melanogaster Engrailed Homeodomain shows a melting temperature increase of 15.5 K. Furthermore, NOMELT achieves zero-shot predictive capabilities in ranking experimental melting and half-activation temperatures across a number of protein families. It achieves this without requiring extensive homology data or massive training datasets as do existing zero-shot predictors by specifically learning thermophilicity, as opposed to all natural variation. These findings underscore the potential of leveraging organismal growth temperatures in context-dependent design of proteins for enhanced thermal stability.

Scientific ReportsVol. 15(1)
Santa Clara University (US), University of Washington (US)
National Science Foundation, University of Washington, National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 92%
Protein Structure and Dynamics
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Neural network conditioned to produce thermophilic protein sequences can increase thermal stability — Evan Komp, Michelle E. McCully, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS