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Knowledge Representation of G-Protein-Coupled Receptor Signal Transduction Pathways

机译:G蛋白偶联受体信号转导途径的知识表示。

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G-protein-coupled receptors (GPCRs) are the largest family of plasma membrane receptors, which can be activated by an external signal such as a ligand. Binding of GPCRs and ligands in the plasma membrane activates pathways that involve a sequence of events. Better understanding of GPCRs and the signal transduction pathways can help biologists to target new drugs or regulate many important cellular functions for diseases. In this paper, we introduce ontology-based GPCR signal transduction pathways, which are converted from manually collected pathways in PubMed papers. We applied network graph embedding and knowledge graph embedding algorithms on the pathway data to discover protein interactions in the GPCR signal transduction pathways. Experiments show that we could suggest missing or unknown pathways by analyzing the ontology-based GPCR signal transduction pathways. Moreover, we introduced ontology constraints on the GPCR pathway for predicting the missing interactions. The experimental results showed that using ontology constraints can boost the performance of knowledge graph embedding algorithms.
机译:G蛋白偶联受体(GPCR)是质膜受体的最大家族,可以被诸如配体的外部信号激活。 GPCR和配体在质膜中的结合激活了涉及一系列事件的途径。更好地了解GPCR和信号转导途径可以帮助生物学家靶向新药或调节疾病的许多重要细胞功能。在本文中,我们介绍了基于本体的GPCR信号转导途径,这些途径是从PubMed论文中的手动收集途径转换而来的。我们在通路数据上应用了网络图嵌入和知识图嵌入算法,以发现GPCR信号转导通路中的蛋白质相互作用。实验表明,通过分析基于本体的GPCR信号转导途径,我们可能会建议缺少或未知的途径。此外,我们在GPCR途径上引入了本体约束,以预测缺失的相互作用。实验结果表明,使用本体约束可以提高知识图嵌入算法的性能。

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