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TGFα 脱落分析:一种准确且通用的检测 GPCR 激活的方法。

TGFα shedding assay: an accurate and versatile method for detecting GPCR activation.

机构信息

Laboratory of Molecular and Cellular Biochemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.

出版信息

Nat Methods. 2012 Oct;9(10):1021-9. doi: 10.1038/nmeth.2172. Epub 2012 Sep 16.

Abstract

A single-format method to detect multiple G protein-coupled receptor (GPCR) signaling, especially Gα(12/13) signaling, presently has limited throughput and sensitivity. Here we report a transforming growth factor-α (TGFα) shedding assay, in which GPCR activation is measured as ectodomain shedding of a membrane-bound proform of alkaline phosphatase-tagged TGFα (AP-TGFα) and its release into conditioned medium. AP-TGFα shedding response occurred almost exclusively downstream of Gα(12/13) and Gα(q) signaling. Relying on chimeric Gα proteins and promiscuous Gα(16) protein, which can couple with Gα(s)- and Gα(i)-coupled GPCRs and induce Gα(q) signaling, we used the TGFα shedding assay to detect 104 GPCRs among 116 human GPCRs. We identified three orphan GPCRs (P2Y10, A630033H20 and GPR174) as Gα(12/13)-coupled lysophosphatidylserine receptors. Thus, the TGFα shedding assay is useful for studies of poorly characterized Gα(12/13)-coupled GPCRs and is a versatile platform for detecting GPCR activation including searching for ligands of orphan GPCRs.

摘要

一种用于检测多种 G 蛋白偶联受体(GPCR)信号,尤其是 Gα(12/13)信号的单格式方法,目前其通量和灵敏度有限。在这里,我们报告了一种转化生长因子-α(TGFα)脱落测定法,其中 GPCR 激活被测量为碱性磷酸酶标记的 TGFα(AP-TGFα)的膜结合前体的细胞外结构域脱落及其释放到条件培养基中。AP-TGFα 脱落反应几乎仅发生在 Gα(12/13)和 Gα(q)信号的下游。利用嵌合 Gα 蛋白和混杂的 Gα(16)蛋白,它们可以与 Gα(s)-和 Gα(i)-偶联的 GPCR 结合并诱导 Gα(q)信号,我们使用 TGFα 脱落测定法检测了 116 个人类 GPCR 中的 104 个 GPCR。我们鉴定出三个孤儿 GPCR(P2Y10、A630033H20 和 GPR174)为 Gα(12/13)-偶联的溶血磷脂酰丝氨酸受体。因此,TGFα 脱落测定法可用于研究表征不佳的 Gα(12/13)-偶联 GPCR,并且是一种用于检测 GPCR 激活的多功能平台,包括寻找孤儿 GPCR 配体。

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