Aug 2026· IEEE journal of biomedical and health informatics· Vol PP· 0 citations
Medicine
TL;DR
The proposed MSIGR-PLA is an integrative framework that integrates local multi-scale interaction features with global protein-ligand representations to improve the accuracy of PLA prediction and consistently outperforms existing methods on four benchmark datasets.
Abstract
Accurate prediction of protein-ligand affinity (PLA) is crucial for accelerating drug discovery. Current methods exhibit limitations in extracting local protein-ligand interaction features and global representations, thereby hindering predictive accuracy. To address these limitations, we propose MSIGR-PLA, an integrative framework that integrates local multi-scale interaction features with global protein-ligand representations to improve the accuracy of PLA prediction. MSIGR-PLA employs two feature encoders to obtain rich representations. The local feature encoder contains a multi-scale dynamic interaction (MSDI) module, which consists of a GCN module, a cross-attention mechanism, and a Graph Transformer module. The global feature encoder uses a pre-trained ESM-2 model to extract protein sequence features and employs a CNN-Transformer module to encode ligand sequence information and a pre-trained GIN module to encode ligand structural information. Experimental results demonstrate that MSIGR-PLA consistently outperforms existing methods on four benchmark datasets, achieving improvements of 3.7%-9.0% in the Pearson correlation coefficient (R). Ablation studies further validate the effectiveness of the key modules in improving overall performance. Additionally, a case study demonstrates that the MSDI module can adaptively model multi-scale interaction features to identify key binding residues around ligands. Our code is available at https://github.com/zhc-moushang/MSIGR-PLA.
The resulting model, HydrAffinity, is an interaction-free, dynamic sparse model that uses pre-trained encoders and MoE for parameter-efficient learning and outperforms all interaction-free methods and matches state-of-the-art interaction-based methods on CASF-2016.
The results demonstrate the effectiveness of integrating multi-scale and multi-modal representations with cross-scale alignment for protein–RNA affinity prediction, and suggest that M2-PRNet can highlight relevant RNA-binding regions and support preliminary discrimination between strong and weak binders when plausible complex structures are available.
Junkai Wang, G. Luo, Yun-Song Yang et al.· Bioinformatics· 0 citations
Accurate prediction of drug-target binding affinity (DTA) is a key task in virtual screening. However, current computational methods face a key challenge: sequence-based approaches often fail to capture critical spatial information, while structure-based models rely on computationally expensive 3D coordinates, which restrict their scalability. To address this issue, we propose StructuraDTA, a novel multimodal framework that adopts an implicit structure modeling strategy. Instead of using static protein folding data, our method encodes drug molecular graphs via Graph Isomorphism Networks (GINs) to capture fine-grained topological features. Meanwhile, we optimize protein representations by integrating probabilistic structural priors into a pretrained language model, which effectively simulates thermodynamic conformational flexibility without relying on explicit 3D structural data. A bidirectional cross-attention mechanism is then used to dynamically align these heterogeneous feature modalities. Comprehensive evaluations on the Davis and KIBA benchmark datasets show that StructuraDTA stably outperforms state of-the-art comparison methods. Importantly, the model exhibits strong robustness in cold-start scenarios, and can accurately predict binding affinities for previously unseen drugs and targets. By retaining the predictive performance of structure based models while maintaining the high inference efficiency of sequence-based methods, we provide an accurate and scalable solution to accelerate genome-scale drug discovery research.
Junlin Xu, Ye Yuan, Menglong Hu et al.· IEEE journal of biomedical a...· 0 citations
CoAff-DTI is proposed, an end-to-end deep learning framework designed to enhance multi-scale interaction modeling for DTI prediction and consistently outperforms state-of-the-art methods on multiple benchmark datasets.
Jia Peng, Xiaoyu Liu, Lei Wang et al.· Journal of Biomedical Inform...· 0 citations
MultiGeo is a DTA prediction framework that explicitly leverages multiple protein conformations rather than a single snapshot, and introduces a disagreement-aware gating mechanism that adaptively fuses this ensemble representation with the dominant structure only when the additional conformers provide complementary information.
Ruida Zeng, Cheng Guo, Yajie Meng et al.· 0 citations