Abstract
BackgroundProtein-protein interactions(PPIs) engage in dynamic pathological and biological procedures constantly in our life. Thus, it is crucial to comprehend the PPIs thoroughly such that we are able to illuminate the disease occurrence, achieve the optimal drug-target therapeutic effect and describe the protein complex structures. However, compared to the protein sequences obtainable from various species and organisms, the number of revealed protein-protein interactions is relatively limited. To address this dilemma, lots of research endeavor have investigated in it to facilitate the discovery of novel PPIs. Among these methods, PPI prediction techniques that merely rely on protein sequence data are more widespread than other methods which require extensive biological domain knowledge.ResultsIn this paper, we propose a multi-modal deep representation learning structure by incorporating protein physicochemical features with the graph topological features from the PPI networks. Specifically, our method not only bears in mind the protein sequence information but also discerns the topological representations for each protein node in the PPI networks. In our paper, we construct a stacked auto-encoder architecture together with a continuous bag-of-words (CBOW) model based on generated metapaths to study the PPI predictions. Following by that, we utilize the supervised deep neural networks to identify the PPIs and classify the protein families. The PPI prediction accuracy for eight species ranged from 96.76% to 99.77%, which signifies that our multi-modal deep representation learning framework achieves superior performance compared to other computational methods.ConclusionTo the best of our knowledge, this is the first multi-modal deep representation learning framework for examining the PPI networks.
Highlights
Protein-protein interactions(PPIs) engage in dynamic pathological and biological procedures constantly in our life
During the stacked auto-encoder (SAE) training phase, we use the mean squared error(MSE) as the loss function defined in Eq 15
For the hprd. org/ (HPRD) dataset, we can see from the results that the mean Receiver operating characteristics (ROC) score achieves 0.9942, which is consistent with other species in the Database of Interacting Proteins (DIP) dataset
Summary
Protein-protein interactions(PPIs) engage in dynamic pathological and biological procedures constantly in our life. Compared to the protein sequences obtainable from various species and organisms, the number of revealed protein-protein interactions is relatively limited. To address this dilemma, lots of research endeavor have investigated in it to facilitate the discovery of novel PPIs. To address this dilemma, lots of research endeavor have investigated in it to facilitate the discovery of novel PPIs Among these methods, PPI prediction techniques that merely rely on protein sequence data are more widespread than other methods which require extensive biological domain knowledge
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