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This study introduces an orthogonal projection method to interpret protein language model (PLM) embeddings by isolating the contribution of specific biochemical properties to fitness predictions. The approach reveals that known tabular features explain a significant portion of the variance in PLM outputs, offering a computationally efficient way to demystify these black-box representations without requiring retraining. By quantifying how biochemical patterns drive downstream performance, this work advances the interpretability of foundation models in computational biology.
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Interpreting Protein Language Model Embeddings via Orthogonal Projection for Protein Fitness Prediction

arXiv3 min read

arXiv:2608.25548v1 Announce Type: new Abstract: Recently, there has been a growing adoption of protein language models (PLMs) in biomedical science. Their embeddings provide a rich numerical representation of protein sequences which achieve state-of-the-art performance on several downstream tasks including protein fitness prediction. However, PLM embeddings are not directly interpretable and, thereby, it remains unclear what features they encode. To gain insight into which biochemical properties of the protein are driving the prediction, we leverage an orthogonal projection technique that removes linear effects of known tabular features from embeddings and extend it to high-order and interaction effects. In this way, we remove the effects of interpretable biochemical features from PLM embeddings. In an ablation study, we show that this leads to a decrease in performance for a downstream classifier trained only on the embeddings to predict protein fitness. In an additional evaluation, we find that these biochemical features explain a substantial part of the variance in the predictions of this classifier. Hence, we can show that PLM embeddings encode patterns correlated with biochemical properties and quantify their contribution to predicting protein fitness. This computationally efficient approach is not limited to the features or embeddings considered here and is readily transferable to problem settings beyond protein fitness prediction.

Abstract:Recently, there has been a growing adoption of protein language models (PLMs) in biomedical science. Their embeddings provide a rich numerical representation of protein sequences which achieve state-of-the-art performance on several downstream tasks including protein fitness prediction. However, PLM embeddings are not directly interpretable and, thereby, it remains unclear what features they encode. To gain insight into which biochemical properties of the protein are driving the prediction, we leverage an orthogonal projection technique that removes linear effects of known tabular features from embeddings and extend it to high-order and interaction effects. In this way, we remove the effects of interpretable biochemical features from PLM embeddings. In an ablation study, we show that this leads to a decrease in performance for a downstream classifier trained only on the embeddings to predict protein fitness. In an additional evaluation, we find that these biochemical features explain a substantial part of the variance in the predictions of this classifier. Hence, we can show that PLM embeddings encode patterns correlated with biochemical properties and quantify their contribution to predicting protein fitness. This computationally efficient approach is not limited to the features or embeddings considered here and is readily transferable to problem settings beyond protein fitness prediction.

Machine Learning (cs.LG); Quantitative Methods (q-bio.QM)

arXiv:2608.25548 [cs.LG]

(or arXiv:2608.25548v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2608.25548 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 298 words

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