Language models have enabled a new era of biological sequence modeling. However, extracting meaningful sequence-level embeddings from these models remains challenging. In this work, we introduce ProteinCLIP, which applies contrastive learning between a protein’s amino acid sequence and curated text describing its function. ProteinCLIP thus learns to take a pre-trained protein language model’s sequence embedding and refines it produce a function-centric embedding. We show that this embedding space yields sequence representations that enable state-of-the-art performance across a variety of important yet challenging tasks in the study of proteins – from predicting protein protein interactions to accurately detecting homologous proteins despite low sequence similarity. More broadly, ProteinCLIP demonstrates the effectiveness of multi-modal learning in biological contexts, and how such strategies can help isolate key signals from large models and further improve their utility.
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Wu et al. (2024) studied this question.
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