首页> 外文OA文献 >The G protein-coupled receptor heterodimer network (GPCR-HetNet) and its hub components
【2h】

The G protein-coupled receptor heterodimer network (GPCR-HetNet) and its hub components

机译:G蛋白偶联受体异二聚体网络(GPCR-HetNet)及其中枢组件

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

G protein-coupled receptors (GPCRs) oligomerization has emerged as a vital characteristic of receptor structure. Substantial experimental evidence supports the existence of GPCR-GPCR interactions in a coordinated and cooperative manner. However, despite the current development of experimental techniques for large-scale detection of GPCR heteromers, in order to understand their connectivity it is necessary to develop novel tools to study the global heteroreceptor networks. To provide insight into the overall topology of the GPCR heteromers and identify key players, a collective interaction network was constructed. Experimental interaction data for each of the individual human GPCR protomers was obtained manually from the STRING and SCOPUS databases. The interaction data were used to build and analyze the network using Cytoscape software. The network was treated as undirected throughout the study. It is comprised of 156 nodes, 260 edges and has a scale-free topology. Connectivity analysis reveals a significant dominance of intrafamily versus interfamily connections. Most of the receptors within the network are linked to each other by a small number of edges. DRD2, OPRM, ADRB2, AA2AR, AA1R, OPRK, OPRD and GHSR are identified as hubs. In a network representation 10 modules/clusters also appear as a highly interconnected group of nodes. Information on this GPCR network can improve our understanding of molecular integration. GPCR-HetNet has been implemented in Java and is freely available at http://www.iiia.csic.es/~ismel/GPCR-Nets/index.html. © 2014 by the authors; licensee MDPI, Basel, Switzerland.
机译:G蛋白偶联受体(GPCR)寡聚已成为受体结构的重要特征。大量的实验证据支持以协同合作的方式存在GPCR-GPCR相互作用。然而,尽管当前已开发出用于大规模检测GPCR异源异构体的实验技术,但为了了解它们的连通性,有必要开发新颖的工具来研究全球异源受体网络。为了深入了解GPCR异构体的整体拓扑结构并确定关键参与者,构建了一个集体相互作用网络。从STRING和SCOPUS数据库手动获得了每个人GPCR原型启动子的实验相互作用数据。使用Cytoscape软件将交互数据用于构建和分析网络。在整个研究过程中,该网络均被视为非定向网络。它由156个节点,260个边组成,并具有无比例缩放拓扑。连接性分析显示,家庭内部连接与家庭之间连接的优势明显。网络中的大多数受体通过少量边缘相互链接。 DRD2,OPRM,ADRB2,AA2AR,AA1R,OPRK,OPRD和GHSR被标识为集线器。在网络表示中,10个模块/集群也显示为高度互连的节点组。有关此GPCR网络的信息可以增进我们对分子整合的了解。 GPCR-HetNet已用Java实现,可从http://www.iiia.csic.es/~ismel/GPCR-Nets/index.html免费获得。 ©2014作者瑞士巴塞尔的MDPI许可证持有者。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号