SA-MPNN：一种面向序列的ThermoMPNN模型，用于精准预测突变对蛋白质热力学稳定性的影响

Abstract

Predicting the impact of single-point mutations on protein thermodynamic stability is crucial for protein engineering of therapeutic and industrial applications. By effectively capturing the three-dimensional structural information of proteins and the spatial physical environment of each residue, the inverse folding models (IFMs) upon fine-tuning, such as ThermoMPNN, achieved state-of-the-art performance in predicting thermostability changes in proteins caused by mutations. However, IFMs are limited in their capacity to capture protein deep evolutionary information, whereas protein language models (pLMs) excel. Here, we present SA-MPNN, a lightweight, end-to-end hybrid framework that dynamically integrates the protein sequence representations from a protein language model (ESM2) into the ThermoMPNN architecture to improve protein stability prediction by combining evolutionary representations with geometric structural embeddings. By evaluating various feature fusion strategies, we selected a self-attention-based integration mechanism to effectively combine the two modalities. Trained on the large-scale Megascale data set, SA-MPNN achieved modest but consistent gains over ThermoMPNN on various benchmark data sets, with particularly noticeable improvements in several correlation analysis and screening-oriented evaluations. Finally, wet-lab validation was performed on the top-ranking variants of Acetivibrio thermocellus β -glucosidase (AtBgl1A) as a case study. The experimental results demonstrated that multiple designed mutants exhibited improved thermostability, and the optimal variant, GC20, achieved a melting temperature ( T m ) of 76.98 ° C, representing a 5.97 ° C increase over the wild-type, thereby supporting the practical applicability of SA-MPNN in protein engineering.