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体内组装和大规模纯化具有 Gβγ 的 GPCR-Gα 融合蛋白,并对活性复合物进行表征。

In vivo assembly and large-scale purification of a GPCR - Gα fusion with Gβγ, and characterization of the active complex.

机构信息

Department of Biochemistry, University of Zürich, Zürich, Switzerland.

出版信息

PLoS One. 2019 Jan 8;14(1):e0210131. doi: 10.1371/journal.pone.0210131. eCollection 2019.

Abstract

G protein coupled receptors (GPCRs) are central players in recognizing a variety of stimuli to mediate diverse cellular responses. This myriad of functions is accomplished by their modular interactions with downstream intracellular transducers, such as heterotrimeric G proteins and arrestins. Assembling a specific GPCR-G protein pair as a purified complex for their structural and functional investigations remains a challenging task, however, because of the low affinity of the interaction. Here, we optimized fusion constructs of the Gα subunit of the heterotrimeric G protein and engineered versions of rat Neurotensin receptor 1 (NTR1), coexpressed and assembled in vivo with Gβ and Gγ. This was achieved by using the baculovirus-based MultiBac system. We thus generated a functional receptor-G protein fusion complex, which can be efficiently purified using ligand-based affinity chromatography on large scales. Additionally, we utilized a purification method based on a designed ankyrin repeat protein tightly binding to Green Fluorescent Protein (GFP-DARPin) that may be used as a generic approach for a large-scale purification of GPCR-G protein fusion complexes for which no ligands column can be generated. The purification methods described herein will support future studies that aim to understand the structural and functional framework of GPCR activation and signaling.

摘要

G 蛋白偶联受体 (GPCRs) 是识别各种刺激物以介导多种细胞反应的核心分子。它们通过与下游细胞内转导蛋白(如异三聚体 G 蛋白和 arrestin)的模块化相互作用来实现这一复杂的功能。然而,由于相互作用的亲和力较低,将特定的 GPCR-G 蛋白对组装为纯化复合物进行结构和功能研究仍然是一项具有挑战性的任务。在这里,我们通过使用基于杆状病毒的 MultiBac 系统,优化了异三聚体 G 蛋白的 Gα 亚基和工程化的大鼠神经降压素受体 1(NTR1)的融合构建体,这些构建体在体内与 Gβ 和 Gγ 共表达和组装。我们因此生成了一种功能性的受体-G 蛋白融合复合物,可以使用基于配体的亲和层析在大规模上进行高效纯化。此外,我们利用一种基于与绿色荧光蛋白(GFP-DARPin)紧密结合的设计锚蛋白重复蛋白的纯化方法,该方法可作为一种通用方法,用于大规模纯化无法生成配体柱的 GPCR-G 蛋白融合复合物。本文所述的纯化方法将支持旨在理解 GPCR 激活和信号转导的结构和功能框架的未来研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c7/6324789/cc52eb743802/pone.0210131.g001.jpg

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