Evidence map›Paper›PMID 27454775›Full record

ArticleBMC bioinformatics2016

A method for predicting protein complex in dynamic PPI networks.

Yijia Zhang, Hongfei Lin, Zhihao Yang, Jian Wang, Yiwei Liu, Shengtian Sang

Abstract read
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Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

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20citing papers in PubMed
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3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Article
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  8. Interactome of Arabidopsis Thaliana.Plants (Basel, Switzerland) · 2022
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yijia ZhangCollege of Computer Science and Technology, Dalian University of Technology Dalian, Liaoning, China. zhyj@dlut.edu.cn.
Hongfei LinCollege of Computer Science and Technology, Dalian University of Technology Dalian, Liaoning, China.
Zhihao YangCollege of Computer Science and Technology, Dalian University of Technology Dalian, Liaoning, China.
Jian WangCollege of Computer Science and Technology, Dalian University of Technology Dalian, Liaoning, China.
Yiwei LiuCollege of Computer Science and Technology, Dalian University of Technology Dalian, Liaoning, China.
Shengtian SangCollege of Computer Science and Technology, Dalian University of Technology Dalian, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate determination of protein complexes has become a key task of system biology for revealing cellular organization and function. Up to now, the protein complex prediction methods are mostly focused on static protein protein interaction (PPI) networks. However, cellular systems are highly dynamic and responsive to cues from the environment. The shift from static PPI networks to dynamic PPI networks is essential to accurately predict protein complex.

resultsThe gene expression data contains crucial dynamic information of proteins and PPIs, along with high-throughput experimental PPI data, are valuable for protein complex prediction. Firstly, we exploit gene expression data to calculate the active time point and the active probability of each protein and PPI. The dynamic active information is integrated into high-throughput PPI data to construct dynamic PPI networks. Secondly, a novel method for predicting protein complexes from the dynamic PPI networks is proposed based on core-attachment structural feature. Our method can effectively exploit not only the dynamic active information but also the topology structure information based on the dynamic PPI networks.

conclusionsWe construct four dynamic PPI networks, and accurately predict many well-characterized protein complexes. The experimental results show that (i) the dynamic active information significantly improves the performance of protein complex prediction; (ii) our method can effectively make good use of both the dynamic active information and the topology structure information of dynamic PPI networks to achieve state-of-the-art protein complex prediction capabilities.

Indexed as

AlgorithmsProtein Interaction MapsComputational BiologyProtein Interaction MappingProteinsTranscriptomeProteins

Identifiers

PMID27454775
PMCPMC4965712

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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.