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β-抑制蛋白的募集促进了与G蛋白的直接结合。

β-arrestin recruitment facilitates a direct association with G proteins.

作者信息

Lee Claudia Y, Smith Jeffrey S, Kohlmann Taylor, Meara Emily M, Pham Uyen, Kwarcinski Frank, Dates Andrew N, Choi Issac, Hilibrand Ari S, Gillikin Abigail, Blacklow Stephen C, Tall Gregory G, Kruse Andrew C, Rajagopal Sudarshan

机构信息

Department of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.

Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

bioRxiv. 2025 Jul 1:2025.06.24.661366. doi: 10.1101/2025.06.24.661366.

Abstract

G protein-coupled receptors (GPCRs) are targets for almost a third of all FDA-approved drugs. GPCRs are known to signal through both heterotrimeric G proteins and β-arrestins. Traditionally these pathways were viewed as largely separable, with G proteins primarily initiating downstream signaling while β-arrestins modulate receptor trafficking and desensitization in addition to regulating their own signaling events. Recent studies suggest an integrated role of G proteins and β-arrestins in GPCR signaling, however the cellular and biochemical requirements for G protein: β-arrestin interactions remain unclear. Here we show that G proteins and β-arrestins can directly interact. Through utilization of β-arrestin-biased receptors and artificially enforced β-arrestin relocalization, we demonstrate that recruitment of β-arrestin to the plasma membrane is sufficient to interact with the G protein Gαi. Using purified proteins, we show that Gαi directly interacts with β-arrestin. In addition, we find that Gαi family members differ in their degree of association with β-arrestin, and that a large degree of this selectivity resides within the alpha helical domain of Gαi. These findings delineate the cellular and biochemical conditions that drive direct interactions between G proteins and β-arrestins and illuminate the molecular basis for how they work together to effect GPCR signaling.

摘要

G蛋白偶联受体(GPCRs)是几乎三分之一的FDA批准药物的作用靶点。已知GPCRs通过异源三聚体G蛋白和β-抑制蛋白进行信号传导。传统上,这些途径在很大程度上被视为可分离的,G蛋白主要启动下游信号传导,而β-抑制蛋白除了调节自身的信号传导事件外,还调节受体转运和脱敏。然而,最近的研究表明G蛋白和β-抑制蛋白在GPCR信号传导中具有整合作用,但是G蛋白与β-抑制蛋白相互作用的细胞和生化要求仍不清楚。在这里,我们表明G蛋白和β-抑制蛋白可以直接相互作用。通过利用偏向β-抑制蛋白的受体和人为强制β-抑制蛋白重新定位,我们证明将β-抑制蛋白募集到质膜足以与G蛋白Gαi相互作用。使用纯化的蛋白,我们表明Gαi直接与β-抑制蛋白相互作用。此外,我们发现Gαi家族成员与β-抑制蛋白的结合程度不同,并且这种选择性很大程度上存在于Gαi的α螺旋结构域内。这些发现描绘了驱动G蛋白和β-抑制蛋白之间直接相互作用的细胞和生化条件,并阐明了它们如何共同作用以影响GPCR信号传导的分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90c1/12236855/aafc84b6a87a/nihpp-2025.06.24.661366v1-f0001.jpg

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