A deep learning architecture for protein-protein Interaction Article identification

Author(s):  
Shweta ◽  
Asif Ekbal ◽  
Sriparna Saha ◽  
Pushpak Bhattacharyya
2021 ◽  
Author(s):  
Lei Deng ◽  
Wenjuan Nie ◽  
Jiaojiao Zhao ◽  
Jingpu Zhang

Abstract Background: Viral infection and diseases are caused by various viruses involved in the protein-protein interaction (PPI) between virus and host, which are a threat to human health. Studying the virus-host PPI is beneficial to apprehending the mechanism of viral infection and developing new treatment drugs. Although several computational methods for predicting the virus-host PPI have been proposed, most of them are supported by the machine learning algorithms, making the hidden high-level feature difficult to be extracted. Results: We proposed a novel hybrid deep learning framework combined with four CNN layers and LSTM to predict the virus-host PPI only using protein sequence information. CNN can extract the nonlinear position-related features of protein sequence, and LSTM can obtain the long-term relevant information. L1-regularized logistic regression is applied to eliminate the noise and redundant information. Our model achieved the best performance on the benchmark dataset and independent set compared with other existing methods. Conclusion: Our method, through the hybrid deep neural network, is useful for predicting virus-host PPI using protein sequence alone, and achieved the best prediction performance compared with other existing methods, which is promising on the virus-host PPI prediction


Author(s):  
Yiwei Li ◽  
Lucian Ilie

AbstractMotivationProteins usually perform their functions by interacting with other proteins, which is why accurately predicting protein-protein interaction (PPI) binding sites is a fundamental problem. Experimental methods are slow and expensive. Therefore, great efforts are being made towards increasing the performance of computational methods.ResultsWe propose DELPHI (DEep Learning Prediction of Highly probable protein Interaction sites), a new sequence-based deep learning suite for PPI binding sites prediction. DELPHI has an ensemble structure with data augmentation and it employs novel features in addition to existing ones. We comprehensively compare DELPHI to nine state-of-the-art programs on five datasets and show that it is more accurate.AvailabilityThe trained model, source code for training, predicting, and data processing are freely available at https://github.com/lucian-ilie/DELPHI. All datasets used in this study can be downloaded at http://www.csd.uwo.ca/~ilie/DELPHI/[email protected]


2021 ◽  
Vol 12 ◽  
Author(s):  
Pan Wang ◽  
Guiyang Zhang ◽  
Zu-Guo Yu ◽  
Guohua Huang

Knowledge about protein-protein interactions is beneficial in understanding cellular mechanisms. Protein-protein interactions are usually determined according to their protein-protein interaction sites. Due to the limitations of current techniques, it is still a challenging task to detect protein-protein interaction sites. In this article, we presented a method based on deep learning and XGBoost (called DeepPPISP-XGB) for predicting protein-protein interaction sites. The deep learning model served as a feature extractor to remove redundant information from protein sequences. The Extreme Gradient Boosting algorithm was used to construct a classifier for predicting protein-protein interaction sites. The DeepPPISP-XGB achieved the following results: area under the receiver operating characteristic curve of 0.681, a recall of 0.624, and area under the precision-recall curve of 0.339, being competitive with the state-of-the-art methods. We also validated the positive role of global features in predicting protein-protein interaction sites.


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