Scoring protein-ligand binding structures through learning atomic graphs with inter-molecular adjacency

With a burgeoning number of artificial intelligence (AI) applications in various fields, biomolecular science has also given a big welcome to advanced AI techniques in recent years. In this broad field, scoring a protein-ligand binding structure to output the binding strength is a crucial problem that heavily relates to computational drug discovery. Aiming at this problem, we have proposed an efficient scoring framework using deep learning techniques. This framework describes a binding structure by a high-resolution atomic graph, places a focus on the inter-molecular interactions and learns the graph in a rational way. For a protein-ligand binding complex, the generated atomic graph reserves key information of the atoms (as graph nodes), and focuses on inter-molecular interactions (as graph edges) that can be identified by introducing multiple distance ranges to the atom pairs within the binding area. To provide more confidence in the predicted binding strengths, we have interpreted the deep learning model from the model level and in a post-hoc analysis. The proposed learning framework has been demonstrated to have competitive performance in scoring and screening tasks, which will prospectively promote the development of related fields further.

Authors

Publication Details

Journal
PLoS Computational Biology
Published
2025-05-09
DOI
https://doi.org/10.1371/journal.pcbi.1013074
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.50

Funders

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article

Scoring protein-ligand binding structures through learning atomic graphs with inter-molecular adjacency

Debby D. Wang, Yuting Huang
1 citations
PLoS Computational Biology
Computational Drug Discovery Methods
1.50
article

Scoring protein-ligand binding structures through learning atomic graphs with inter-molecular adjacency

Debby D. Wang, Yuting Huang
article en
1 citations

Abstract

With a burgeoning number of artificial intelligence (AI) applications in various fields, biomolecular science has also given a big welcome to advanced AI techniques in recent years. In this broad field, scoring a protein-ligand binding structure to output the binding strength is a crucial problem that heavily relates to computational drug discovery. Aiming at this problem, we have proposed an efficient scoring framework using deep learning techniques. This framework describes a binding structure by a high-resolution atomic graph, places a focus on the inter-molecular interactions and learns the graph in a rational way. For a protein-ligand binding complex, the generated atomic graph reserves key information of the atoms (as graph nodes), and focuses on inter-molecular interactions (as graph edges) that can be identified by introducing multiple distance ranges to the atom pairs within the binding area. To provide more confidence in the predicted binding strengths, we have interpreted the deep learning model from the model level and in a post-hoc analysis. The proposed learning framework has been demonstrated to have competitive performance in scoring and screening tasks, which will prospectively promote the development of related fields further.

PLoS Computational BiologyVol. 21(5)
Research Grants Council, University Grants Committee
Openalex Percentile: Top 17%
Computational Drug Discovery Methods
1.50
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