ProtAlign: Contrastive learning paradigm for Sequence and structure alignment
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Abstract (arXiv)
Protein language models often take into consideration the alignment between a protein sequence and its textual description. However, they do not take structural information into consideration. Traditional methods treat sequence and structure separately, limiting the ability to exploit the alignment between the structure and protein sequence embeddings. In this paper, we introduce a sequence structure contrastive alignment framework, which learns a shared embedding space where proteins are represented consistently across modalities. By training on large-scale pairs of sequences and experimentally resolved or predicted structures, the model maximizes agreement between matched sequence structure pairs while pushing apart unrelated pairs. This alignment enables cross-modal retrieval (e.g., finding structural neighbors given a sequence), improves downstream prediction tasks such as function annotation and stability estimation, and provides interpretable links between sequence variation and structural organization. Our results demonstrate that contrastive learning can serve as a powerful bridge between protein sequences and structures, offering a unified representation for understanding and engineering proteins.
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References · 8
- 2017Attention Is All You Needcited by 59,932
- 2021Learning Transferable Visual Models From Natural Language Supervisioncited by 33,456
- 2023LLaMA: Open and Efficient Foundation Language Modelscited by 13,958
- 2016Layer Normalizationcited by 5,579
- 2023Sigmoid Loss for Language Image Pre-Trainingcited by 3,048
- 2023ProtST: Multi-Modality Learning of Protein Sequences and Biomedical Textscited by 78
- 2024EvoLlama: Enhancing LLMs' Understanding of Proteins via Multimodal Structure and Sequence Representationscited by 9
- 2024ProtCLIP: Function-Informed Protein Multi-Modal Learningcited by 6
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- 2024Sequence-Augmented SE(3)-Flow Matching For Conditional Protein Backbone Generation
- 2025ProtTeX: Structure-In-Context Reasoning and Editing of Proteins with Large Language Models
- 2025Understanding protein function with a multimodal retrieval-augmented foundation model
- 2024TourSynbio: A Multi-Modal Large Model and Agent Framework to Bridge Text and Protein Sequences for Protein Engineering
- 2026Protein Language Models Diverge from Natural Language: Comparative Analysis and Improved Inference