scholarly journals Graph embedding-based novel protein interaction prediction via higher-order graph convolutional network

PLoS ONE ◽  
2020 ◽  
Vol 15 (9) ◽  
pp. e0238915 ◽  
Author(s):  
Ze Xiao ◽  
Yue Deng
Author(s):  
Guofeng Lv ◽  
Zhiqiang Hu ◽  
Yanguang Bi ◽  
Shaoting Zhang

The study of multi-type Protein-Protein Interaction (PPI) is fundamental for understanding biological processes from a systematic perspective and revealing disease mechanisms. Existing methods suffer from significant performance degradation when tested in unseen dataset. In this paper, we investigate the problem and find that it is mainly attributed to the poor performance for inter-novel-protein interaction prediction. However, current evaluations overlook the inter-novel-protein interactions, and thus fail to give an instructive assessment. As a result, we propose to address the problem from both the evaluation and the methodology. Firstly, we design a new evaluation framework that fully respects the inter-novel-protein interactions and gives consistent assessment across datasets. Secondly, we argue that correlations between proteins must provide useful information for analysis of novel proteins, and based on this, we propose a graph neural network based method (GNN-PPI) for better inter-novel-protein interaction prediction. Experimental results on real-world datasets of different scales demonstrate that GNN-PPI significantly outperforms state-of-the-art PPI prediction methods, especially for the inter-novel-protein interaction prediction.


PLoS Genetics ◽  
2021 ◽  
Vol 17 (11) ◽  
pp. e1009869
Author(s):  
Jiajun Qiu ◽  
Kui Chen ◽  
Chunlong Zhong ◽  
Sihao Zhu ◽  
Xiao Ma

The perturbations of protein-protein interactions (PPIs) were found to be the main cause of cancer. Previous PPI prediction methods which were trained with non-disease general PPI data were not compatible to map the PPI network in cancer. Therefore, we established a novel cancer specific PPI prediction method dubbed NECARE, which was based on relational graph convolutional network (R-GCN) with knowledge-based features. It achieved the best performance with a Matthews correlation coefficient (MCC) = 0.84±0.03 and an F1 = 91±2% compared with other methods. With NECARE, we mapped the cancer interactome atlas and revealed that the perturbations of PPIs were enriched on 1362 genes, which were named cancer hub genes. Those genes were found to over-represent with mutations occurring at protein-macromolecules binding interfaces. Furthermore, over 56% of cancer treatment-related genes belonged to hub genes and they were significantly related to the prognosis of 32 types of cancers. Finally, by coimmunoprecipitation, we confirmed that the NECARE prediction method was highly reliable with a 90% accuracy. Overall, we provided the novel network-based cancer protein-protein interaction prediction method and mapped the perturbation of cancer interactome. NECARE is available at: https://github.com/JiajunQiu/NECARE.


Methods ◽  
2016 ◽  
Vol 110 ◽  
pp. 64-72 ◽  
Author(s):  
Kai Tian ◽  
Mingyu Shao ◽  
Yang Wang ◽  
Jihong Guan ◽  
Shuigeng Zhou

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