Identification of Protein Complexes from Tandem Affinity Purification/Mass Spectrometry Data via Biased Random Walk

被引:5
|
作者
Cai, Bingjing [1 ]
Wang, Haiying [1 ]
Zheng, Huiru [1 ]
Wang, Hui [1 ]
机构
[1] Univ Ulster, Comp Sci Res Inst, Sch Comp & Math, Coleraine BT52 1SA, Londonderry, North Ireland
关键词
Protein-protein interaction network; tandem affinity purification/mass spectrometry; protein complexes; random walk with restart; FUNCTIONAL MODULES; GENE ONTOLOGY; INTERACTOME; NETWORKS;
D O I
10.1109/TCBB.2014.2352616
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Systematic identification of protein complexes from protein-protein interaction networks (PPIs) is an important application of data mining in life science. Over the past decades, various new clustering techniques have been developed based on modelling PPIs as binary relations. Non-binary information of co-complex relations (prey/bait) in PPIs data derived from tandem affinity purification/mass spectrometry (TAP-MS) experiments has been unfairly disregarded. In this paper, we propose a Biased Random Walk based algorithm for detecting protein complexes from TAP-MS data, resulting in the random walk with restarting baits (RWRB). RWRB is developed based on Random walk with restart. The main contribution of RWRB is the incorporation of co-complex relations in TAP-MS PPI networks into the clustering process, by implementing a new restarting strategy during the process of random walk. Through experimentation on un-weighted and weighted TAP-MS data sets, we validated biological significance of our results by mapping them to manually curated complexes. Results showed that, by incorporating non-binary, co-membership information, significant improvement has been achieved in terms of both statistical measurements and biological relevance. Better accuracy demonstrates that the proposed method outperformed several state-of-the-art clustering algorithms for the detection of protein complexes in TAP-MS data.
引用
收藏
页码:455 / 466
页数:12
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