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{"title":"Bioluminescence Resonance Energy Transfer Assay to Characterize Gi-Like G Protein Subtype-Dependent Functional Selectivity","authors":"Hideaki Yano, Marta Sánchez-Soto, Sergi Ferré","doi":"10.1002/cpns.38","DOIUrl":null,"url":null,"abstract":"<p>G protein–coupled receptors (GPCRs) comprise the single most targeted protein class in pharmacology. G protein signaling transduces extracellular stimuli such as neurotransmitters into cellular responses. Although preference for a specific GPCR among different G protein families (e.g., Gs-, Gi-, or Gq-like proteins) is often well studied, preference for a specific G protein subtype (e.g., Gi1, Gi2, Gi3, Go1, and Go2) has received little attention. Due to tissue expression differences and potentially exploitable functional differences, G protein subtype-dependent functional selectivity is an attractive framework to expand GPCR drug development. Herein we present a bioluminescence resonance energy transfer (BRET)-based method to characterize functional selectivity among Gi-like protein subtypes. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":40016,"journal":{"name":"Current Protocols in Neuroscience","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpns.38","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpns.38","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Neuroscience","Score":null,"Total":0}
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Abstract
G protein–coupled receptors (GPCRs) comprise the single most targeted protein class in pharmacology. G protein signaling transduces extracellular stimuli such as neurotransmitters into cellular responses. Although preference for a specific GPCR among different G protein families (e.g., Gs-, Gi-, or Gq-like proteins) is often well studied, preference for a specific G protein subtype (e.g., Gi1, Gi2, Gi3, Go1, and Go2) has received little attention. Due to tissue expression differences and potentially exploitable functional differences, G protein subtype-dependent functional selectivity is an attractive framework to expand GPCR drug development. Herein we present a bioluminescence resonance energy transfer (BRET)-based method to characterize functional selectivity among Gi-like protein subtypes. © 2017 by John Wiley & Sons, Inc.
生物发光共振能量转移试验表征gi样G蛋白亚型依赖的功能选择性
G蛋白偶联受体(gpcr)是药理学中最具靶向性的一类蛋白。G蛋白信号转导细胞外刺激如神经递质进入细胞反应。尽管不同G蛋白家族(如Gs-、Gi-或gq样蛋白)对特定GPCR的偏好经常得到很好的研究,但对特定G蛋白亚型(如Gi1、Gi2、Gi3、Go1和Go2)的偏好却很少得到关注。由于组织表达差异和潜在可利用的功能差异,G蛋白亚型依赖的功能选择性是扩大GPCR药物开发的一个有吸引力的框架。在此,我们提出了一种基于生物发光共振能量转移(BRET)的方法来表征gi样蛋白亚型之间的功能选择性。©2017 by John Wiley &儿子,Inc。
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