通过检测酿酒酵母蛋白质相互作用网络中的拓扑和功能簇来鉴定必需蛋白质

Kaustav Sengupta, Sovan Saha, P. Chatterjee, M. Kundu, M. Nasipuri, Subhadip Basu
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引用次数: 1

摘要

必需蛋白鉴定是检查疾病进展机制和确定药物靶点的重要因素。随着高通量基因组测序项目的推进,大量的蛋白质数据可以用于相互作用模式的分析、功能注释和表征,以检测蛋白质在网络层面的必要性。一组中心性测量被用来识别高度连接的蛋白质或枢纽。从最近的研究中可以观察到,大多数枢纽被认为是必需的蛋白质。在本文中,提出了一种方法EPIN_Pred,其中使用几种中心性度量的组合来查找中心蛋白和非中心蛋白。利用内聚性,找到了重叠的拓扑簇。使用基因本体(GO)术语,如果需要,这些拓扑簇再次组合。与其他最先进的方法相比,EPIN_Pred的性能也更优越。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Essential Proteins by Detecting Topological and Functional Clusters in Protein Interaction Network of Saccharomyces Cerevisiae
Essential protein identification is an important factor to inspect the mechanisms of disease progression and to identify drug targets. With the advancement of high throughput genome sequencing projects, a bulk of protein data is available where the analysis of interaction pattern, functional annotation and characterization are necessary for detecting proteins' essentiality in network level. A set of centrality measure has been used to identify the highly connected proteins or hubs. From recent studies, it is observed that the majority of hubs are considered to be essential proteins. In this article, a method EPIN_Pred is proposed where a combination of several centrality measures is used to find the hub and non-hub proteins. Using the cohesiveness property, overlapping topological clusters are found. Using gene ontology (GO) terms, these topological clusters are again combined, if required. The performance of EPIN_Pred is also found to be superior when compared to other state-of-the-art methods.
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