AUTHOR=Gao Xu , Yan Mengfan , Zhang Chengwei , Wu Gang , Shang Jiandong , Zhang Congxiang , Yang Kecheng 

TITLE=MDNN-DTA: a multimodal deep neural network for drug-target affinity prediction

JOURNAL=Frontiers in Genetics

VOLUME=Volume 16 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1527300

DOI=10.3389/fgene.2025.1527300

ISSN=1664-8021

ABSTRACT=Determining drug-target affinity (DTA) is a pivotal step in drug discovery, where in silico methods can significantly improve efficiency and reduce costs. Artificial intelligence (AI), especially deep learning models, can automatically extract high-dimensional features from the biological sequences of drug molecules and target proteins. This technology demonstrates lower complexity in DTA prediction compared to traditional experimental methods, particularly when handling large-scale data. In this study, we introduce a multimodal deep neural network model for DTA prediction, referred to as MDNN-DTA. This model employs Graph Convolutional Networks (GCN) and Convolutional Neural Networks (CNN) to extract features from the drug and protein sequences, respectively. One notable strength of our method is its ability to accurately predict DTA directly from the sequences of the target proteins, obviating the need for protein 3D structures, which are frequently unavailable in drug discovery. To comprehensively extract features from the protein sequence, we leverage an ESM pre-trained model for extracting biochemical features and design a specific Protein Feature Extraction (PFE) block for capturing both global and local features of the protein sequence. Furthermore, a Protein Feature Fusion (PFF) Block is engineered to augment the integration of multi-scale protein features derived from the abovementioned techniques. We then compare MDNN-DTA with other models on the same dataset, conducting a series of ablation experiments to assess the performance and efficacy of each component. The results highlight the advantages and effectiveness of the MDNN-DTA method.