Evidence map›Paper›PMID 40059137›Full record

ArticleBMC bioinformatics2025

Constructing multilayer PPI networks based on homologous proteins and integrating multiple PageRank to identify essential proteins.

He Zhao, Huan Xu, Tao Wang, Guixia Liu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

He ZhaoCollege of Computer Science and Technology, Jilin University, Changchun, China.
Huan XuCollege of Computer Science and Technology, Jilin University, Changchun, China.
Tao WangCollege of Computer Science and Technology, Jilin University, Changchun, China.
Guixia LiuCollege of Computer Science and Technology, Jilin University, Changchun, China. liugx@jlu.edu.cn.

Funding

National Natural Science Foundation of China 62372208Science and Technology Development Program of Jilin Province YD ZJ202501ZYTS325
6 · The paper itself

Abstract

backgroundPredicting and studying essential proteins not only helps to understand the fundamental requirements for cell survival and growth regulation mechanisms but also deepens our understanding of disease mechanisms and drives drug development. Existing methods for identifying essential proteins primarily focus on PPI networks within a single species, without fully exploiting interspecies homologous relationships. These homologous relationships connect proteins from different species, forming multilayer PPI networks. Some methods only construct interlayer edges based on homologous relationships between two species, without incorporating appropriate biological attributes to assess the biological significance of these edges. Furthermore, homologous proteins are often highly conserved across multiple species, and expanding homologous relationships to more species allows for a more accurate assessment of interlayer edge importance.

resultsTo address these issues, we propose a novel model, MLPR, which constructs a multilayer PPI network based on homologous proteins and integrates multiple PageRank algorithms to identify essential proteins. This study combines homologous protein data from three species to construct interlayer transition matrices and assigns weights to interlayer edges by integrating the biological attributes of homologous proteins and cross-species GO annotations. The MLPR model uses multiple PageRank methods to comprehensively consider homologous relationships across species and designs three key parameters to find the optimal combination that balances random walks within layers, global jumps, interlayer biases, and interspecies homologous relationships.

conclusionsExperimental results show that MLPR outperforms other state-of-the-art methods in terms of performance. Ablation experiments further validate that integrating homologous relationships across three species effectively enhances the overall performance of MLPR and demonstrates the advantages of the multiple PageRank model in identifying essential proteins.

Indexed as

Computational BiologyProtein Interaction MappingProtein Interaction MapsProteinsAlgorithmsAnimalsDatabases, ProteinProteinsEssential proteinsHomologous proteinsMultilayer PPI networksMultiple PageRank

Identifiers

PMID40059137
PMCPMC11892321

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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.