PIGNet: A physics-informed deep learning model toward generalized drug-target interaction predictions
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Abstract (arXiv)
Recently, deep neural network (DNN)-based drug-target interaction (DTI) models were highlighted for their high accuracy with affordable computational costs. Yet, the models' insufficient generalization remains a challenging problem in the practice of in-silico drug discovery. We propose two key strategies to enhance generalization in the DTI model. The first is to predict the atom-atom pairwise interactions via physics-informed equations parameterized with neural networks and provides the total binding affinity of a protein-ligand complex as their sum. We further improved the model generalization by augmenting a broader range of binding poses and ligands to training data. We validated our model, PIGNet, in the comparative assessment of scoring functions (CASF) 2016, demonstrating the outperforming docking and screening powers than previous methods. Our physics-informing strategy also enables the interpretation of predicted affinities by visualizing the contribution of ligand substructures, providing insights for further ligand optimization.
Key facts. Cited by 31 papers in the map (data through 7 Oct 2026). First posted on arXiv 22 Aug 2020.
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Citing papers per year: 2022: 8; 2023: 9; 2024: 6; 2025: 6; 2026: 2.
31 papers.
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- 2022DiffDock: Diffusion Steps, Twists, and Turns for Molecular Dockingcited by 307
- 2022Multimodal learning with graphscited by 54
- 2022Structure-based drug design with geometric deep learningcited by 40
- 2022Bidirectional Generation of Structure and Properties Through a Single Molecular Foundation Modelcited by 25
- 2023Unsupervised Protein-Ligand Binding Energy Prediction via Neural Euler's Rotation Equationcited by 18
- 2023Protein-ligand binding representation learning from fine-grained interactionscited by 12
- 2022SS-GNN: A Simple-Structured Graph Neural Network for Affinity Predictioncited by 7
- 2023Multi-task Bioassay Pre-training for Protein-ligand Binding Affinity Predictioncited by 7
- 2023GeoTMI:Predicting quantum chemical property with easy-to-obtain geometry via positional denoisingcited by 5
- 2024A Cross-Field Fusion Strategy for Drug-Target Interaction Predictioncited by 5
- 2022Learning Physics-Consistent Particle Interactionscited by 4
- 2022Associative Learning Mechanism for Drug-Target Interaction Predictioncited by 4
19 more
- 2023PharmacoNet: Accelerating Large-Scale Virtual Screening by Deep Pharmacophore Modelingcited by 4
- 2023Improved prediction of ligand-protein binding affinities by meta-modelingcited by 3
- 2024Binding Affinity Prediction: From Conventional to Machine Learning-Based Approachescited by 3
- 2025Advances in Protein Representation Learning: Methods, Applications, and Future Directionscited by 3
- 2023Geometric Deep Learning for Structure-Based Drug Design: A Surveycited by 2
- 2023PGraphDTA: Improving Drug Target Interaction Prediction using Protein Language Models and Contact Mapscited by 2
- 2024MIN: Multi-channel Interaction Network for Drug-Target Interaction with Protein Distillationcited by 2
- 2022High Performance of Gradient Boosting in Binding Affinity Predictioncited by 1
- 2024QuickBind: A Light-Weight And Interpretable Molecular Docking Modelcited by 1
- 2025Preferential Multi-Objective Bayesian Optimization for Drug Discoverycited by 1
- 2025A comprehensive analysis of PINNs: Variants, Applications, and Challengescited by 1
- 2025ToxBench: A Binding Affinity Prediction Benchmark with AB-FEP-Calculated Labels for Human Estrogen Receptor Alphacited by 1
- 2025Contrastive Multi-Task Learning with Solvent-Aware Augmentation for Drug Discoverycited by 1
- 2023DiffDTM: A conditional structure-free framework for bioactive molecules generation targeted for dual proteinscited by 0
- 2024DualBind: A Dual-Loss Framework for Protein-Ligand Binding Affinity Predictioncited by 0
- 2024SPIN: SE(3)-Invariant Physics Informed Network for Binding Affinity Predictioncited by 0
- 2025Global Universal Scaling and Ultra-Small Parameterization in Machine Learning Interatomic Potentials with Super-Linearitycited by 0
- 2026BioLM-Score: Language-Prior Conditioned Probabilistic Geometric Potentials for Protein-Ligand Scoringcited by 0
- 2026RAVEN: Frozen Random Graph Reservoirs with Physics-Informed Interaction Fingerprints for Protein-Ligand Binding Affinity Predictioncited by 0
- 2026RAVEN: Frozen Random Graph Reservoirs with Physics-Informed Interaction Fingerprints for Protein-Ligand Binding Affinity Prediction10 Aug 2026
- 2026BioLM-Score: Language-Prior Conditioned Probabilistic Geometric Potentials for Protein-Ligand Scoring9 Feb 2026
- 2025Contrastive Multi-Task Learning with Solvent-Aware Augmentation for Drug Discovery3 Aug 2025
- 2025ToxBench: A Binding Affinity Prediction Benchmark with AB-FEP-Calculated Labels for Human Estrogen Receptor Alpha11 Jul 2025
- 2025A comprehensive analysis of PINNs: Variants, Applications, and Challenges28 May 2025
- 2025Preferential Multi-Objective Bayesian Optimization for Drug Discovery21 Mar 2025
- 2025Advances in Protein Representation Learning: Methods, Applications, and Future Directions20 Mar 2025
- 2025Global Universal Scaling and Ultra-Small Parameterization in Machine Learning Interatomic Potentials with Super-Linearity11 Feb 2025
- 2024MIN: Multi-channel Interaction Network for Drug-Target Interaction with Protein Distillation23 Nov 2024
- 2024QuickBind: A Light-Weight And Interpretable Molecular Docking Model21 Oct 2024
- 2024Binding Affinity Prediction: From Conventional to Machine Learning-Based Approaches30 Sep 2024
- 2024SPIN: SE(3)-Invariant Physics Informed Network for Binding Affinity Prediction10 Jul 2024
19 more
- 2024DualBind: A Dual-Loss Framework for Protein-Ligand Binding Affinity Prediction11 Jun 2024
- 2024A Cross-Field Fusion Strategy for Drug-Target Interaction Prediction23 May 2024
- 2023Protein-ligand binding representation learning from fine-grained interactions9 Nov 2023
- 2023PGraphDTA: Improving Drug Target Interaction Prediction using Protein Language Models and Contact Maps6 Oct 2023
- 2023Improved prediction of ligand-protein binding affinities by meta-modeling5 Oct 2023
- 2023PharmacoNet: Accelerating Large-Scale Virtual Screening by Deep Pharmacophore Modeling1 Oct 2023
- 2023DiffDTM: A conditional structure-free framework for bioactive molecules generation targeted for dual proteins24 Jun 2023
- 2023Geometric Deep Learning for Structure-Based Drug Design: A Survey20 Jun 2023
- 2023Multi-task Bioassay Pre-training for Protein-ligand Binding Affinity Prediction8 Jun 2023
- 2023GeoTMI:Predicting quantum chemical property with easy-to-obtain geometry via positional denoising28 Mar 2023
- 2023Unsupervised Protein-Ligand Binding Energy Prediction via Neural Euler's Rotation Equation25 Jan 2023
- 2022Bidirectional Generation of Structure and Properties Through a Single Molecular Foundation Model19 Nov 2022
- 2022Structure-based drug design with geometric deep learning19 Oct 2022
- 2022DiffDock: Diffusion Steps, Twists, and Turns for Molecular Docking4 Oct 2022
- 2022Multimodal learning with graphs7 Sep 2022
- 2022SS-GNN: A Simple-Structured Graph Neural Network for Affinity Prediction25 May 2022
- 2022Associative Learning Mechanism for Drug-Target Interaction Prediction24 May 2022
- 2022High Performance of Gradient Boosting in Binding Affinity Prediction14 May 2022
- 2022Learning Physics-Consistent Particle Interactions1 Feb 2022
- 2022DiffDock: Diffusion Steps, Twists, and Turns for Molecular Dockingcited by 307
- 2022Multimodal learning with graphscited by 54
- 2022Structure-based drug design with geometric deep learningcited by 40
- 2022Bidirectional Generation of Structure and Properties Through a Single Molecular Foundation Modelcited by 25
- 2023Unsupervised Protein-Ligand Binding Energy Prediction via Neural Euler's Rotation Equationcited by 18
- 2023Protein-ligand binding representation learning from fine-grained interactionscited by 12
- 2022SS-GNN: A Simple-Structured Graph Neural Network for Affinity Predictioncited by 7
- 2023Multi-task Bioassay Pre-training for Protein-ligand Binding Affinity Predictioncited by 7
- 2023GeoTMI:Predicting quantum chemical property with easy-to-obtain geometry via positional denoisingcited by 5
- 2024A Cross-Field Fusion Strategy for Drug-Target Interaction Predictioncited by 5
- 2022Learning Physics-Consistent Particle Interactionscited by 4
- 2022Associative Learning Mechanism for Drug-Target Interaction Predictioncited by 4
12 most cited of 31 All 31 (JSON)
- 2026RAVEN: Frozen Random Graph Reservoirs with Physics-Informed Interaction Fingerprints for Protein-Ligand Binding Affinity Prediction10 Aug 2026
- 2026BioLM-Score: Language-Prior Conditioned Probabilistic Geometric Potentials for Protein-Ligand Scoring9 Feb 2026
- 2025Contrastive Multi-Task Learning with Solvent-Aware Augmentation for Drug Discovery3 Aug 2025
- 2025ToxBench: A Binding Affinity Prediction Benchmark with AB-FEP-Calculated Labels for Human Estrogen Receptor Alpha11 Jul 2025
- 2025A comprehensive analysis of PINNs: Variants, Applications, and Challenges28 May 2025
- 2025Preferential Multi-Objective Bayesian Optimization for Drug Discovery21 Mar 2025
- 2025Advances in Protein Representation Learning: Methods, Applications, and Future Directions20 Mar 2025
- 2025Global Universal Scaling and Ultra-Small Parameterization in Machine Learning Interatomic Potentials with Super-Linearity11 Feb 2025
- 2024MIN: Multi-channel Interaction Network for Drug-Target Interaction with Protein Distillation23 Nov 2024
- 2024QuickBind: A Light-Weight And Interpretable Molecular Docking Model21 Oct 2024
- 2024Binding Affinity Prediction: From Conventional to Machine Learning-Based Approaches30 Sep 2024
- 2024SPIN: SE(3)-Invariant Physics Informed Network for Binding Affinity Prediction10 Jul 2024
12 newest of 31 All 31 (JSON)