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Progressive Multi-Modality Learning for Inverse Protein Folding
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While deep generative models show promise for learning inverse protein folding directly from data, the lack of publicly available structure-sequence pairings limits their generalization. Previous improvements and data augmentation efforts to overcome this bottleneck have been insufficient. To further address this challenge, we propose a novel protein design paradigm called MMDesign, which leverages multi-modality transfer learning. To our knowledge, MMDesign is the first framework that combines a pretrained structural module with a pretrained contextual module, using an auto-encoder (AE) based language model to incorporate prior protein semantic knowledge. Experimental results, only training with the small dataset, demonstrate that MMDesign consistently outperforms baselines on various public benchmarks. To further assess the biological plausibility, we present systematic quantitative analysis techniques that provide interpretability and reveal more about the laws of protein design.
Forward citations
Cited by 2 Pith papers
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DapPep: Domain Adaptive Peptide-agnostic Learning for Universal T-cell Receptor-antigen Binding Affinity Prediction
DapPep, built from ESM-2 with cross-attention and peptide-reconstruction pre-training, reports ROC-AUC 0.816 and PR-AUC 0.836 on unseen peptides, beating PanPep by about 9 to 11 percent.
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Pan-protein Design Learning Enables Task-adaptive Generalization for Low-resource Enzyme Design
CrossDesign aligns pretrained protein language models with structure encoders to improve enzyme sequence design and zero-shot mutation fitness prediction.
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