Discovering essential proteins based on PPI network and protein complex

被引:23
|
作者
Ren, Jun [1 ,2 ]
Wang, Jianxin [1 ]
Li, Min [1 ]
Wu, Fangxiang [3 ,4 ]
机构
[1] Cent S Univ, Sch Informat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Hunan Agr Univ, Coll Informat Sci & Technol, Changsha 410128, Hunan, Peoples R China
[3] Univ Saskatchewan, Dept Mech Engn, Saskatoon, SK S7N 5A9, Canada
[4] Univ Saskatchewan, Div Biomed Engn, Saskatoon, SK S7N 5A9, Canada
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
centrality measure; complex centrality; essential proteins; harmonic centrality; PPI network; protein complex; SACCHAROMYCES-CEREVISIAE; CENTRALITY; GENOME; IDENTIFICATION; ACCURACY; GENES;
D O I
10.1504/IJDMB.2015.068951
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Most computational methods for identifying essential proteins focus on the topological centrality of protein-protein interaction (PPI) networks. However, these methods have limitations, such as the difficulty for identifying essential proteins with low centrality values and the poor performance for incomplete PPI network. In this paper, protein complex is proven to be an important factor for determining protein essentiality and a new centrality measure, complex centrality, is proposed. The weighted average of complex centrality and subgraph centrality, called harmonic centrality (HC), is proposed to predict essential proteins. It combines PPI network topology and protein complex information and has better performance than methods based on PPI network. The improvement is higher when the PPI network is incomplete. Furthermore, a weighted PPI network is generated by integrating cellular localisation and biological process to a PPI network. The performance of HC measure is improved 5% in this weighted PPI network.
引用
收藏
页码:24 / 43
页数:20
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