Identification of Protein Complexes Based on Core-Attachment Structure and Combination of Centrality Measures and Biological Properties in PPI Weighted Networks

In protein interaction networks, a complex is a group of proteins that causes a biological process to take place. The correct identification of complexes can help to better understand function of cells used for therapeutic purposes, such as drug discoveries. This paper uses core-attachment structure, centrality measures, and biological properties of proteins to identify protein complex with the aim of enhancing prediction accuracy compared to related work. We used theinherentorganization of complex to the identification in this article, while most methods have not considered such properties. On the other hand, clustering methods, as the common method for identifying complexes in protein interaction networks have been applied. However, we want to propose a method for more accurate identification of complexes in this article. Using this method, we determined the core center of each complex and its attachment proteins using the centrality measures, biological properties and weight density, whereby the weight of each interaction was calculated using the protein information in the gene ontology. In the proposed approach to weighting the network and measuring the importance of proteins, we used our previous work. To compare with other methods, we used datasets DIP, Collins, Krogan, and Human. The results show that the performance of our method was significantly improved, compared to other methods, in terms of detecting the protein complex. Using the p-value concept, we show the biological significance of our predicted complexes. The proposed method could identify an acceptable number of protein complexes, with the highest proportion of biological significance in collaborating on the functional annotation of proteins.