Determination of GPCR Phosphorylation Status: Establishing a Phosphorylation Barcode.

Q2 Pharmacology, Toxicology and Pharmaceutics
Rudi Prihandoko, Sophie J Bradley, Andrew B Tobin, Adrian J Butcher
{"title":"Determination of GPCR Phosphorylation Status: Establishing a Phosphorylation Barcode.","authors":"Rudi Prihandoko,&nbsp;Sophie J Bradley,&nbsp;Andrew B Tobin,&nbsp;Adrian J Butcher","doi":"10.1002/0471141755.ph0213s69","DOIUrl":null,"url":null,"abstract":"<p><p>G protein-coupled receptors (GPCRs) are rapidly phosphorylated following agonist occupation in a process that mediates receptor uncoupling from its cognate G protein, a process referred to as desensitization. In addition, this process provides a mechanism by which receptors can engage with arrestin adaptor molecules and couple to downstream signaling pathways. The importance of this regulatory process has been highlighted recently by the understanding that ligands can direct receptor signaling along one pathway in preference to another, the phenomenon of signaling bias that is partly mediated by the phosphorylation status or phosphorylation barcode of the receptor. Methods to determine the phosphorylation status of a GPCR in vitro and in vivo are necessary to understand not only the physiological mechanisms involved in GPCR signaling, but also to fully examine the signaling properties of GPCR ligands. This unit describes detailed methods for determining the overall phosphorylation pattern on a receptor (the phosphorylation barcode), as well as mass spectrometry approaches that can define the precise sites that become phosphorylated. These techniques, coupled with the generation and characterization of receptor phosphorylation-specific antibodies, provide a full palate of techniques necessary to determine the phosphorylation status of any given GPCR subtype.</p>","PeriodicalId":10871,"journal":{"name":"Current Protocols in Pharmacology","volume":"69 ","pages":"2.13.1-2.13.26"},"PeriodicalIF":0.0000,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/0471141755.ph0213s69","citationCount":"21","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/0471141755.ph0213s69","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 21

Abstract

G protein-coupled receptors (GPCRs) are rapidly phosphorylated following agonist occupation in a process that mediates receptor uncoupling from its cognate G protein, a process referred to as desensitization. In addition, this process provides a mechanism by which receptors can engage with arrestin adaptor molecules and couple to downstream signaling pathways. The importance of this regulatory process has been highlighted recently by the understanding that ligands can direct receptor signaling along one pathway in preference to another, the phenomenon of signaling bias that is partly mediated by the phosphorylation status or phosphorylation barcode of the receptor. Methods to determine the phosphorylation status of a GPCR in vitro and in vivo are necessary to understand not only the physiological mechanisms involved in GPCR signaling, but also to fully examine the signaling properties of GPCR ligands. This unit describes detailed methods for determining the overall phosphorylation pattern on a receptor (the phosphorylation barcode), as well as mass spectrometry approaches that can define the precise sites that become phosphorylated. These techniques, coupled with the generation and characterization of receptor phosphorylation-specific antibodies, provide a full palate of techniques necessary to determine the phosphorylation status of any given GPCR subtype.

测定GPCR磷酸化状态:建立磷酸化条形码。
G蛋白偶联受体(gpcr)在激动剂占据后迅速磷酸化,介导受体与其同源G蛋白解偶联,这一过程称为脱敏。此外,这一过程还提供了一种机制,通过这种机制,受体可以与抑制素适配器分子结合,并偶联到下游信号通路。这一调节过程的重要性最近得到了强调,因为人们认识到配体可以沿着一条途径优先于另一条途径指导受体信号传导,这种信号偏倚现象部分由受体的磷酸化状态或磷酸化条形码介导。确定GPCR在体外和体内磷酸化状态的方法,不仅是了解GPCR信号传导的生理机制,而且是全面研究GPCR配体信号传导特性的必要条件。本单元详细介绍了确定受体总体磷酸化模式(磷酸化条形码)的方法,以及可以定义被磷酸化的精确位点的质谱方法。这些技术,加上受体磷酸化特异性抗体的产生和表征,提供了确定任何给定GPCR亚型磷酸化状态所需的完整技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Current Protocols in Pharmacology
Current Protocols in Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信