Sequence-Free for Compound Protein Interaction Prediction
Hongzhi Zhang, Jiameng Chen, Kun Li, Yida Xiong, Xiantao Cai, Wenbin Hu, Jia Wu
摘要
The prediction of compound–protein interactions (CPIs) is crucial for drug discovery. Most existing CPI prediction models rely on protein sequence information as input. However, in early-stage drug development, particularly in phenotype-driven studies or compound-response analyses, proteins are often annotated only with functional labels, and their sequences remain undetermined. Consequently, current methods are inapplicable in such scenarios. Furthermore, our experiments find that even when large-scale perturbations were applied to protein sequences, the predictive performance of the existing models did not show a significant decline. It indicates that the high investment in sequencing may not bring corresponding returns. To address the above issues, we propose an inexpensive, protein-sequencing-free framework BioText-CPI, based on the Biomedical Textual description of protein for CPI prediction. Firstly, during the pre-training stage of the model, we use contrastive learning to align protein texts and sequence modalities. Subsequently, we add biological text descriptions of proteins to the existing public CPI dataset to construct a new CPI dataset. Finally, in the CPI prediction stage, the sequence and biomedical text descriptions of proteins can be used as the input for CPI prediction either separately or simultaneously to meet the application requirements of different scenarios. The experiments demonstrate that BioText-CPI achieves comparable effects to the traditional methods when only the biomedical description of protein is input. Moreover, when the two modalities of protein information are input simultaneously, BioText-CPI achieves state-of-the-art performance across multiple scenarios.
问问这篇 Paper
智能体会读完全文。
Lune 把这篇 Paper 索引到了每一个公式,引用它的顶会 Paper 也一样。你提问,回答直接引用原文。
它引用的顶会 Paper6
- Language models enable zero-shot prediction of the effects of mutations on protein functionJoshua Meier, Roshan Rao, Robert Verkuil, Jason Liu 等NeurIPS 2021 · 被引用 969 次
- TANKBind: Trigonometry-Aware Neural NetworKs for Drug-Protein Binding Structure PredictionWei Lu, Qifeng Wu, Jixian Zhang, Jiahua Rao 等NeurIPS 2022 · 被引用 254 次
- ProtST: Multi-Modality Learning of Protein Sequences and Biomedical TextsMinghao Xu, Xinyu Yuan, Santiago Miret, Jian TangICML 2023 · 被引用 147 次
- Improving the Gating Mechanism of Recurrent Neural NetworksAlbert Gu, Çaglar Gülçehre, Thomas Paine, Matt Hoffman 等ICML 2020 · 被引用 111 次
- Knowledge Distillation Improves Graph Structure Augmentation for Graph Neural NetworksLirong Wu, Haitao Lin, Yufei Huang, Stan Z. LiNeurIPS 2022 · 被引用 60 次
相关 Paper
- PSC-CPI: Multi-Scale Protein Sequence-Structure Contrasting for Efficient and Generalizable Compound-Protein Interaction PredictionLirong Wu, Yufei Huang, Cheng Tan, Zhangyang Gao 等AAAI 2024 · 被引用 20 次
- S²Drug: Bridging Protein Sequence and 3D Structure in Contrastive Representation Learning for Virtual ScreeningBowei He, Bowen Gao, Yankai Chen, Yanyan Lan 等AAAI 2026 · 被引用 1 次
- Prot2Text-V2: Protein Function Prediction with Multimodal Contrastive AlignmentXiao Fei, Michail Chatzianastasis, Sarah Almeida Carneiro, Hadi Abdine 等NeurIPS 2025 · 被引用 12 次
- FuseMine: Robust Multi-Modal Compound-Protein Interaction Prediction via Differential Attention Feature MiningJunlin Xu, Zhuang Zhang, Zhenghang Gong, Jincan Li 等AAAI 2026
- GRAM-DTI: Adaptive Multimodal Representation Learning for Drug–Target Interaction PredictionFeng Jiang, Amina Mollaysa, Hehuan Ma, Yuzhi Guo 等ICLR 2026
