Abstract
BackgroundAccurate determination of protein complexes is crucial for understanding cellular organization and function. High-throughput experimental techniques have generated a large amount of protein-protein interaction (PPI) data, allowing prediction of protein complexes from PPI networks. However, the high-throughput data often includes false positives and false negatives, making accurate prediction of protein complexes difficult.MethodThe biomedical literature contains large quantities of PPI data that, along with high-throughput experimental PPI data, are valuable for protein complex prediction. In this study, we employ a natural language processing technique to extract PPI data from the biomedical literature. This data is subsequently integrated with high-throughput PPI and gene ontology data by constructing attributed PPI networks, and a novel method for predicting protein complexes from the attributed PPI networks is proposed. This method allows calculation of the relative contribution of high-throughput and biomedical literature PPI data.ResultsMany well-characterized protein complexes are accurately predicted by this method when apply to two different yeast PPI datasets. The results show that (i) biomedical literature PPI data can effectively improve the performance of protein complex prediction; (ii) our method makes good use of high-throughput and biomedical literature PPI data along with gene ontology data to achieve state-of-the-art protein complex prediction capabilities.
Highlights
Accurate determination of protein complexes is crucial for understanding cellular organization and function
Many well-characterized protein complexes are accurately predicted by this method when apply to two different yeast protein-protein interaction (PPI) datasets
The results show that (i) biomedical literature PPI data can effectively improve the performance of protein complex prediction; (ii) our method makes good use of high-throughput and biomedical literature PPI data along with gene ontology data to achieve state-of-the-art protein complex prediction capabilities
Summary
Accurate determination of protein complexes is crucial for understanding cellular organization and function. High-throughput experimental techniques have generated a large amount of protein-protein interaction (PPI) data, allowing prediction of protein complexes from PPI networks. The high-throughput data often includes false positives and false negatives, making accurate prediction of protein complexes difficult. Protein complexes are formed from two or more associated polypeptide chains, and accurate determination of protein complexes is of great importance for understanding cellular organization and function. Even in the relatively simple model organism Saccharomyces cerevisiae, protein complexes include many subunits that assemble and function in a coherent fashion. A key task of system biology is to understand proteins and their interactions in terms of protein complexes [1]. Nepusz et al proposed the ClusterONE algorithm [11] which detected overlapping protein complexes in PPI networks
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