MIN: Multi-channel Interaction Network for Drug-Target Interaction with Protein Distillation

• URL: http://arxiv.org/abs/2412.07778v1
• Date: Sat, 23 Nov 2024 05:38:36 GMT
• Title: MIN: Multi-channel Interaction Network for Drug-Target Interaction with Protein Distillation
• Authors: Shuqi Li, Shufang Xie, Hongda Sun, Yuhan Chen, Tao Qin, Tianjun Ke, Rui Yan,
• Abstract summary: Multi-channel Interaction Network (MIN) is a novel framework designed to predict drug-target interaction (DTI) MIN incorporates a representation learning module and a multi-channel interaction module. MIN is not only a potent tool for DTI prediction but also offers fresh insights into the prediction of protein binding sites.
• Score: 64.4838301776267
• License:
• Abstract: Traditional drug discovery processes are both time-consuming and require extensive professional expertise. With the accumulation of drug-target interaction (DTI) data from experimental studies, leveraging modern machine-learning techniques to discern patterns between drugs and target proteins has become increasingly feasible. In this paper, we introduce the Multi-channel Interaction Network (MIN), a novel framework designed to predict DTIs through two primary components: a representation learning module and a multi-channel interaction module. The representation learning module features a C-Score Predictor-assisted screening mechanism, which selects critical residues to enhance prediction accuracy and reduce noise. The multi-channel interaction module incorporates a structure-agnostic channel, a structure-aware channel, and an extended-mixture channel, facilitating the identification of interaction patterns at various levels for optimal complementarity. Additionally, contrastive learning is utilized to harmonize the representations of diverse data types. Our experimental evaluations on public datasets demonstrate that MIN surpasses other strong DTI prediction methods. Furthermore, the case study reveals a high overlap between the residues selected by the C-Score Predictor and those in actual binding pockets, underscoring MIN's explainability capability. These findings affirm that MIN is not only a potent tool for DTI prediction but also offers fresh insights into the prediction of protein binding sites.

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