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临近标记法鉴定配体激活的 G 蛋白偶联受体下游的β-arrestin1 结合伴侣

Proximity Labeling to Identify β-Arrestin1 Binding Partners Downstream of Ligand-Activated G Protein-Coupled Receptors.

机构信息

Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Int J Mol Sci. 2023 Feb 7;24(4):3285. doi: 10.3390/ijms24043285.

Abstract

β-arrestins are multifaceted adaptor proteins that regulate various aspects of G protein-coupled receptor (GPCR) signaling. β-arrestins are recruited to agonist-activated and phosphorylated GPCRs at the plasma membrane, thereby preventing G protein coupling, while also targeting GPCRs for internalization via clathrin-coated pits. In addition, β-arrestins can activate various effector molecules to prosecute their role in GPCR signaling; however, the full extent of their interacting partners remains unknown. To discover potentially novel β-arrestin interacting partners, we used APEX-based proximity labeling coupled with affinity purification and quantitative mass spectrometry. We appended APEX in-frame to the C-terminus of β-arrestin1 (βarr1-APEX), which we show does not impact its ability to support agonist-stimulated internalization of GPCRs. By using coimmunoprecipitation, we show that βarr1-APEX interacts with known interacting proteins. Furthermore, following agonist stimulation βarr1-APEX labeled known βarr1-interacting partners as assessed by streptavidin affinity purification and immunoblotting. Aliquots were prepared in a similar manner and analyzed by tandem mass tag labeling and high-content quantitative mass spectrometry. Several proteins were found to be increased in abundance following GPCR stimulation. Biochemical experiments confirmed two novel proteins that interact with β-arrestin1, which we predict are novel ligand-stimulated βarr1 interacting partners. Our study highlights that βarr1-APEX-based proximity labeling represents a valuable approach to identifying novel players involved in GPCR signaling.

摘要

β-arrestins 是多功能衔接蛋白,可调节 G 蛋白偶联受体 (GPCR) 信号的各个方面。β-arrestins 被募集到配体激活和磷酸化的质膜 GPCR 上,从而阻止 G 蛋白偶联,同时通过网格蛋白包被陷窝将 GPCR 靶向内化。此外,β-arrestins 可以激活各种效应分子来发挥其在 GPCR 信号转导中的作用;然而,其相互作用伙伴的全部范围尚不清楚。为了发现潜在的新型β-arrestin 相互作用伙伴,我们使用基于 APEX 的邻近标记与亲和纯化和定量质谱相结合。我们将 APEX 以框内方式附加到β-arrestin1 (βarr1-APEX) 的 C 末端,我们证明这不会影响其支持激动剂刺激的 GPCR 内化的能力。通过共免疫沉淀,我们表明βarr1-APEX 与已知的相互作用蛋白相互作用。此外,在用激动剂刺激后,βarr1-APEX 标记了已知的βarr1 相互作用伙伴,如链霉亲和素亲和纯化和免疫印迹所示。以类似的方式制备等分试样,并通过串联质量标签标记和高内涵定量质谱进行分析。发现几种蛋白质在 GPCR 刺激后丰度增加。生化实验证实了与β-arrestin1 相互作用的两种新型蛋白质,我们预测它们是新型配体刺激的βarr1 相互作用伙伴。我们的研究强调了基于βarr1-APEX 的邻近标记代表了一种识别参与 GPCR 信号转导的新型参与者的有价值的方法。

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