Evidence map›Paper›PMID 40784875›Full record

ArticleBMC biology2025

MESM: integrating multi-source data for high-accuracy protein-protein interactions prediction through multimodal language models.

Feng Wang, Jinming Chu, Liyan Shen, Shan Chang

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Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Feng WangSchool of Computer Science and Artificial Intelligence, Aliyun School of Big Data, School of Software, Changzhou University, Changzhou, 213164, China.
Jinming ChuSchool of Computer Science and Artificial Intelligence, Aliyun School of Big Data, School of Software, Changzhou University, Changzhou, 213164, China.
Liyan ShenSchool of Computer Engineering, Suzhou Vocational University, Suzhou, 215104, China. liyan.shen@jssvc.edu.cn.
Shan ChangInstitute of Bioinformatics and Medical Engineering, School of Electrical and Information Engineering, Jiangsu University of Technology, Changzhou, 213001, China. schang@jsut.edu.cn.

Funding

National Natural Science Foundation of China 62373172
6 · The paper itself

Abstract

backgroundProtein-protein interactions (PPIs) play a critical role in essential biological processes such as signal transduction, enzyme activity regulation, cytoskeletal structure, immune responses, and gene regulation. However, current methods mainly focus on extracting features from protein sequences and using graph neural network (GNN) to acquire interaction information from the PPI network graph. This limits the model's ability to learn richer and more effective interaction information, thereby affecting prediction performance.

resultsIn this study, we propose a novel deep learning method, MESM, for effectively predicting PPI. The datasets used for the PPI prediction task were primarily constructed from the STRING database, including two Homo sapiens PPI datasets, SHS27k and SHS148k, and two Saccharomyces cerevisiae PPI datasets, SYS30k and SYS60k. MESM consists of three key modules, as follows: First, MESM extracts multimodal representations from protein sequence information, protein structure information, and point cloud features through Sequence Variational Autoencoder (SVAE), Variational Graph Autoencoder (VGAE), and PointNet Autoencoder (PAE). Then, Fusion Autoencoder (FAE) is used to integrate these multimodal features, generating rich and balanced protein representations. Next, MESM leverages GraphGPS to learn structural information from the PPI network graph structure and combines Graph Attention Network (GAT) to further capture protein interaction information. Finally, MESM uses Graph Convolutional Network (GCN) and SubgraphGCN to extract global and local features from the perspective of the overall graph and subgraphs. Moreover, we build seven independent graphs from the overall PPI network graph to specifically learn the features of each PPI type, thereby enhancing the model's learning ability for different types of interactions.

conclusionsCompared to the state-of-the-art methods, MESM achieved improvements of 8.77%, 4.98%, 7.48%, and 6.08% on SHS27k, SHS148k, SYS30k, and SYS60k, respectively. The experimental results demonstrate that MESM exhibits significant improvements in PPI prediction performance.

Indexed as

Deep LearningProtein Interaction MappingProtein Interaction MapsDatabases, ProteinHumansNeural Networks, ComputerSaccharomyces cerevisiaeGraph neural networkMultimodal protein feature pre-trainingProtein–protein interaction

Identifiers

PMID40784875
PMCPMC12337455

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.