首页> 外文期刊>Nature reviews neuroscience >Mechanisms of the anterograde trafficking of GPCRs: Regulation of AT1R transport by interacting proteins and motifs
【24h】

Mechanisms of the anterograde trafficking of GPCRs: Regulation of AT1R transport by interacting proteins and motifs

机译:对GPCR的伪造贩运机制:通过相互作用和图案来调节AT1R运输

获取原文
获取原文并翻译 | 示例
       

摘要

Anterograde cell surface transport of nascent G protein-coupled receptors (GPCRs) en route from the endoplasmic reticulum (ER) through the Golgi apparatus represents a crucial checkpoint to control the amount of the receptors at the functional destination and the strength of receptor activation-elicited cellular responses. However, as compared with extensively studied internalization and recycling processes, the molecular mechanisms of cell surface trafficking of GPCRs are relatively less defined. Here, we will review the current advances in understanding the ER-Golgi-cell surface transport of GPCRs and use angiotensin II type 1 receptor as a representative GPCR to discuss emerging roles of receptor-interacting proteins and specific motifs embedded within the receptors in controlling the forward traffic of GPCRs along the biosynthetic pathway.
机译:从内质网(ER)通过GOLGI装置的鼻塞G蛋白偶联受体(GPCR)的胎儿细胞表面传输代表了控制功能目的地的受体量和受体激活引发的强度的关键检查点 细胞反应。 然而,与广泛研究的内化和回收过程相比,细胞表面运输GPCR的分子机制相对较少。 在这里,我们将审查目前在理解GPCR的ER-Golgi-Cell表面传输并使用血管紧张素II型受体作为代表性GPCR,以讨论受体相互作用蛋白和嵌入受体内的特定基序的新兴作用 沿生物合成途径的GPCR的远程流量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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