
FOLLOWUS
Department of Information and Computing Science, Changsha University, Changsha 410003, China
[ "Wen-yin NI, E-mail:masonni@163.com" ]
Sai HU, E-mail:husaiccsu@163.com
收稿:2013-04-03,
修回:2013-;9-23,
纸质出版:2013-10
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Predicting overlapping protein complexes in weighted interactome networks[J]. 信息与电子工程前沿(英文), 2013,14(10):756-765.
Wen-yin NI, Hui-jun XIONG, Bi-hai ZHAO, et al. Predicting overlapping protein complexes in weighted interactome networks[J]. Frontiers of Information Technology & Electronic Engineering, 2013, 14(10): 756-765.
Predicting overlapping protein complexes in weighted interactome networks[J]. 信息与电子工程前沿(英文), 2013,14(10):756-765. DOI: 10.1631/jzus.C13b0097.
Wen-yin NI, Hui-jun XIONG, Bi-hai ZHAO, et al. Predicting overlapping protein complexes in weighted interactome networks[J]. Frontiers of Information Technology & Electronic Engineering, 2013, 14(10): 756-765. DOI: 10.1631/jzus.C13b0097.
Protein complexes play important roles in integrating individual gene products to perform useful cellular functions. The increasing mount of protein–protein interaction (PPI) data has enabled us to predict protein complexes. In spite of the advances in these computational approaches and experimental techniques
it is impossible to construct an absolutely reliable PPI network. Taking into account the reliability of interactions in the PPI network
we have constructed a weighted protein–protein interaction (WPPI) network
in which the reliability of each interaction is represented as a weight using the topology of the PPI network. As overlaps are likely to have biological importance
we proposed a novel method named WN-PC (weighted network-based method for predicting protein complexes) to predict overlapping protein complexes on the WPPI network. The proposed algorithm predicts neighborhood graphs with an aggregation coefficient over a threshold as candidate complexes
and binds attachment proteins to candidate complexes. Finally
we have filtered redundant complexes which overlap other complexes to a very high extent in comparison to their density and size. A comprehensive comparison between competitive algorithms and our WN-PC method has been made in terms of the
F
-measure
coverage rate
and
P
-value. We have applied WN-PC to two different yeast PPI data sets
one of which is a huge PPI network consisting of over 6000 proteins and 200 000 interactions. Experimental results show that WN-PC outperforms the state-of-the-art methods. We think that our research may be helpful for other applications in PPI networks.
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