{"title":"Get Ready to Sharpen Your Tools: A Short Guide to Heterotrimeric G Protein Activity Biosensors.","authors":"Remi Janicot, Mikel Garcia-Marcos","doi":"10.1124/molpharm.124.000949","DOIUrl":null,"url":null,"abstract":"<p><p>G protein-coupled receptors (GPCRs) are the largest class of transmembrane receptors encoded in the human genome, and they initiate cellular responses triggered by a plethora of extracellular stimuli ranging from neurotransmitters and hormones to photons. Upon stimulation, GPCRs activate heterotrimeric G proteins (G<i>αβ</i>γ) in the cytoplasm, which then convey signals to their effectors to elicit cellular responses. Given the broad biological and biomedical relevance of GPCRs and G proteins in physiology and disease, there is great interest in developing and optimizing approaches to measure their signaling activity with high accuracy and across experimental systems pertinent to their functions in cellular communication. This review provides a historical perspective on approaches to measure GPCR-G protein signaling, from quantification of second messengers and other indirect readouts of activity to biosensors that directly detect the activity of G proteins. The latter is the focus of a more detailed overview of the evolution of design principles for various optical biosensors of G protein activity with different experimental capabilities. We will highlight advantages and limitations of biosensors that detect different G protein activation hallmarks, like dissociation of G<i>α</i> and G<i>β</i>γ or nucleotide exchange on G<i>α</i>, as well as their suitability to detect signaling mediated by endogenous versus exogenous signaling components or in physiologically relevant systems like primary cells. Overall, this review intends to provide an assessment of the state-of-the-art for biosensors that directly measure G protein activity to allow readers to make informed decisions on the selection and implementation of currently available tools. SIGNIFICANCE STATEMENT: G protein activity biosensors have become essential and widespread tools to assess GPCR signaling and pharmacology. Yet, investigators face the challenge of choosing from a growing list of G protein activity biosensors. This review provides an overview of the features and capabilities of different optical biosensor designs for the direct detection of G protein activity in cells, with the aim of facilitating the rational selection of systems that align with the specific scientific questions and needs of investigators.</p>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11331509/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1124/molpharm.124.000949","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0
Abstract
G protein-coupled receptors (GPCRs) are the largest class of transmembrane receptors encoded in the human genome, and they initiate cellular responses triggered by a plethora of extracellular stimuli ranging from neurotransmitters and hormones to photons. Upon stimulation, GPCRs activate heterotrimeric G proteins (Gαβγ) in the cytoplasm, which then convey signals to their effectors to elicit cellular responses. Given the broad biological and biomedical relevance of GPCRs and G proteins in physiology and disease, there is great interest in developing and optimizing approaches to measure their signaling activity with high accuracy and across experimental systems pertinent to their functions in cellular communication. This review provides a historical perspective on approaches to measure GPCR-G protein signaling, from quantification of second messengers and other indirect readouts of activity to biosensors that directly detect the activity of G proteins. The latter is the focus of a more detailed overview of the evolution of design principles for various optical biosensors of G protein activity with different experimental capabilities. We will highlight advantages and limitations of biosensors that detect different G protein activation hallmarks, like dissociation of Gα and Gβγ or nucleotide exchange on Gα, as well as their suitability to detect signaling mediated by endogenous versus exogenous signaling components or in physiologically relevant systems like primary cells. Overall, this review intends to provide an assessment of the state-of-the-art for biosensors that directly measure G protein activity to allow readers to make informed decisions on the selection and implementation of currently available tools. SIGNIFICANCE STATEMENT: G protein activity biosensors have become essential and widespread tools to assess GPCR signaling and pharmacology. Yet, investigators face the challenge of choosing from a growing list of G protein activity biosensors. This review provides an overview of the features and capabilities of different optical biosensor designs for the direct detection of G protein activity in cells, with the aim of facilitating the rational selection of systems that align with the specific scientific questions and needs of investigators.
G 蛋白偶联受体(GPCR)是人类基因组中编码的最大一类跨膜受体,从神经递质、激素到光子等大量细胞外刺激都会引发它们启动细胞反应。受到刺激后,GPCRs 会激活细胞质中的异三聚 G 蛋白(Gαβγ),然后将信号传递给效应器,引起细胞反应。鉴于 GPCR 和 G 蛋白在生理学和疾病中广泛的生物学和生物医学相关性,人们对开发和优化方法以高精度测量它们的信号活性以及跨实验系统测量它们在细胞通讯中的功能产生了浓厚的兴趣。本综述从历史的角度介绍了测量 GPCR-G 蛋白信号转导的方法,从量化第二信使和其他间接读出的活性,到直接检测 G 蛋白活性的生物传感器。后者是更详细概述具有不同实验能力的各种 G 蛋白活性光学生物传感器设计原则演变的重点。我们将重点介绍检测不同 G 蛋白活化标志(如 Gα 和 Gβγ 的解离或 Gα 上的核苷酸交换)的生物传感器的优势和局限性,以及它们是否适合检测由内源性和外源性信号成分介导的信号传导,或在原代细胞等生理相关系统中的信号传导。总之,本综述旨在对直接测量 G 蛋白活性的生物传感器的最新技术进行评估,以便读者在选择和使用现有工具时做出明智的决定。意义声明 G 蛋白活性生物传感器已成为评估 GPCR 信号转导和药理学的重要且广泛的工具。然而,研究人员面临着从越来越多的 G 蛋白活性生物传感器中进行选择的挑战。本综述概述了用于直接检测细胞中 G 蛋白活性的不同光学生物传感器设计的特点和功能,旨在帮助研究人员合理选择符合特定科学问题和需求的系统。