...
首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Receptor component protein, an endogenous allosteric modulator of family B G protein coupled receptors
【24h】

Receptor component protein, an endogenous allosteric modulator of family B G protein coupled receptors

机译:受体组分蛋白,家庭B G蛋白偶联受体的内源性颠振调制剂

获取原文
获取原文并翻译 | 示例

摘要

Receptor component protein (RCP) is a 148 amino acid intracellular peripheral membrane protein, previously identified as promoting the coupling of CGRP to CAMP production at the CGRP receptor, a heterodimer of calcitonin receptor like-receptor (CLR), a family B G protein-coupled receptor (GPCR) and receptor activity modifying protein 1 (RAMP1). We extend these observations to show that it selectively enhances CGRP receptor coupling to Gs but not Gq or pERK activation. At other family B GPCRs, it enhances cAMP production at the calcitonin, corticotrophin releasing factor type 1a and glucagon-like peptide type 2 receptors with their cognate ligands but not at the adrenomedullin type 1 (AM(1)), gastric inhibitory peptide and glucagon-like peptide type 1 receptors, all expressed in transfected HEK293S cells. However, there is also cell-line variability as RCP did not enhance CAMP production at the endogenous calcitonin receptor in HEK293T cells and it has previously been reported that it is active on the AM(1) receptor expressed on NIH3T3 cells. RCP appears to behave as a positive allosteric modulator at coupling a number of family B GPCRs to Gs, albeit in a manner that is regulated by cell-specific factors. It may exert its effects at the interface between the 2nd intracellular loop of the GPCR and Gs, although there is likely to be some overlap between this location and that occupied by the C-terminus of RAMPs if they bind to the GPCRs.
机译:受体组分蛋白(RCP)是148个氨基酸细胞内外周膜蛋白,以前鉴定为促进CGRP在CGRP受体的CGRP受体偶联,促进CGRP受体(CLR)的异二二二聚体,蛋白偶联受体(GPCR)和受体活性改性蛋白1(RAMP1)。我们扩展了这些观察结果,表明它选择性地增强了CGRP受体耦合到GS但不是GQ或PERK激活。在其他家庭B GPCR中,它增强了降钙素的CAMP生产,皮质萎缩蛋白释放因子型1A和胰高血糖素样肽2型受体,其具有其同源配体,但不适用于肾上腺素型1(AM(1)),胃抑制肽和胰高血糖素 - 状肽类型1受体,全部在转染的HEK293S细胞中表达。然而,随着RCP在HEK293T细胞中的内源性降钙素受体中没有增强CAMP生产,还存在细胞型变异性,并且先前报道其在NIH3T3细胞上表达的AM(1)受体上是活性的。 RCP似乎表现为正颠arseric调节剂,其在偶联许多家庭B​​ GPCR至GS,尽管以细胞特异性因素调节的方式。它可以在GPCR和GS的第二个细胞内环路之间的界面处发挥其效果,尽管在该位置之间可能存在一些重叠,并且如果它们与GPCR结合而被斜坡的C末端占据。

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