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CCPL: Cross-modal Contrastive Protein Learning

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arxiv 2303.11783 v2 pith:7GJ2MTW6 submitted 2023-03-19 q-bio.BM cs.AIcs.LG

classification q-bio.BMcs.AIcs.LG
keywords proteinlearningstructuralccplcontrastivelanguagemethodspretraining
verification ladder T0 review T1 audit T2 compute T3 formal
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Effective protein representation learning is crucial for predicting protein functions. Traditional methods often pretrain protein language models on large, unlabeled amino acid sequences, followed by finetuning on labeled data. While effective, these methods underutilize the potential of protein structures, which are vital for function determination. Common structural representation techniques rely heavily on annotated data, limiting their generalizability. Moreover, structural pretraining methods, similar to natural language pretraining, can distort actual protein structures. In this work, we introduce a novel unsupervised protein structure representation pretraining method, cross-modal contrastive protein learning (CCPL). CCPL leverages a robust protein language model and uses unsupervised contrastive alignment to enhance structure learning, incorporating self-supervised structural constraints to maintain intrinsic structural information. We evaluated our model across various benchmarks, demonstrating the framework's superiority.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. DapPep: Domain Adaptive Peptide-agnostic Learning for Universal T-cell Receptor-antigen Binding Affinity Prediction

    q-bio.QM 2024-11 conditional novelty 5.0 of 10

    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.

  2. Pan-protein Design Learning Enables Task-adaptive Generalization for Low-resource Enzyme Design

    q-bio.QM 2024-11 conditional novelty 5.0 of 10

    CrossDesign aligns pretrained protein language models with structure encoders to improve enzyme sequence design and zero-shot mutation fitness prediction.

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