Interformer: an interaction-aware model for protein-ligand docking and affinity prediction

In recent years, the application of deep learning models to protein-ligand docking and affinity prediction, both vital for structure-based drug design, has garnered increasing interest. However, many of these models overlook the intricate modeling of interactions between ligand and protein atoms in the complex, consequently limiting their capacity for generalization and interpretability. In this work, we propose Interformer, a unified model built upon the Graph-Transformer architecture. The proposed model is designed to capture non-covalent interactions utilizing an interaction-aware mixture density network. Additionally, we introduce a negative sampling strategy, facilitating an effective correction of interaction distribution for affinity prediction. Experimental results on widely used and our in-house datasets demonstrate the effectiveness and universality of the proposed approach. Extensive analyses confirm our claim that our approach improves performance by accurately modeling specific protein-ligand interactions. Encouragingly, our approach advances docking tasks state-of-the-art (SOTA) performance.

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Publication Details

Journal
Nature Communications
Published
2024-11-25
DOI
https://doi.org/10.1038/s41467-024-54440-6
Citations
34
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
12.29

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article

Interformer: an interaction-aware model for protein-ligand docking and affinity prediction

Houtim Lai, Xiangxiang Zeng, Fang Wu, Geyan Ye et al.
34 citations
Nature Communications
Computational Drug Discovery Methods
12.29
article

Interformer: an interaction-aware model for protein-ligand docking and affinity prediction

Houtim Lai, Xiangxiang Zeng, Fang Wu, Geyan Ye, Fandi Wu, Longyue Wang, Wei Liu, Peng Zhou, Ruiyuan Qian, Junhong Huang
article en
34 citations

Abstract

In recent years, the application of deep learning models to protein-ligand docking and affinity prediction, both vital for structure-based drug design, has garnered increasing interest. However, many of these models overlook the intricate modeling of interactions between ligand and protein atoms in the complex, consequently limiting their capacity for generalization and interpretability. In this work, we propose Interformer, a unified model built upon the Graph-Transformer architecture. The proposed model is designed to capture non-covalent interactions utilizing an interaction-aware mixture density network. Additionally, we introduce a negative sampling strategy, facilitating an effective correction of interaction distribution for affinity prediction. Experimental results on widely used and our in-house datasets demonstrate the effectiveness and universality of the proposed approach. Extensive analyses confirm our claim that our approach improves performance by accurately modeling specific protein-ligand interactions. Encouragingly, our approach advances docking tasks state-of-the-art (SOTA) performance.

Nature CommunicationsVol. 15(1)
Hunan University (CN), Tencent (China) (CN), Stanford University (US)
Tencent
Openalex Percentile: Top 1%
Computational Drug Discovery Methods
12.29
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