Laboratory for GPCR Biology, Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Laboratory for GPCR Biology, Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Graduate Program in Molecular Biophysics and Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Trends Endocrinol Metab. 2019 Nov;30(11):860-874. doi: 10.1016/j.tem.2019.07.011.
The parathyroid hormone (PTH) type 1 receptor (PTHR) is the canonical G protein-coupled receptor (GPCR) for PTH and PTH-related protein (PTHrP) and the key regulator of calcium homeostasis and bone turnover. PTHR function is critical for human health to maintain homeostatic control of ionized serum Ca levels and has several unusual signaling features, such as endosomal cAMP signaling, that are well-studied but not structurally understood. In this review, we discuss how recently solved high resolution near-atomic structures of hormone-bound PTHR in its inactive and active signaling states and discovery of extracellular Ca allosterism shed light on the structural basis for PTHR signaling and function.
甲状旁腺激素(PTH)1 型受体(PTHR)是 PTH 和 PTH 相关蛋白(PTHrP)的经典 G 蛋白偶联受体(GPCR),也是钙稳态和骨代谢的关键调节剂。PTHR 的功能对人类健康至关重要,可维持离子化血清 Ca 水平的体内平衡控制,并且具有几种不寻常的信号特征,如内体 cAMP 信号传导,这些特征已得到很好的研究,但在结构上尚不清楚。在这篇综述中,我们讨论了最近解决的配体结合的 PTHR 处于非活性和活性信号状态的高分辨率近原子结构,以及发现细胞外 Ca 变构作用如何阐明 PTHR 信号转导和功能的结构基础。