Structure and function of the receptor for parathyroid hormone and parathyroid hormone-related protein.

Receptor Pub Date : 1993-01-01
R A Nissenson, Z Huang, E Blind, D Shoback
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Abstract

The receptor for parathyroid hormone (PTH) and PTH-related protein (PTHrP) is a member of a subfamily of G-protein-coupled receptors. This subfamily includes receptors for calcitonin, secretin, vasoactive intestinal polypeptide, glucagon, and related peptides, growth hormone-releasing hormone, and pituitary adenylate cyclase activating peptide. These receptors couple agonist occupancy to activation of adenylate cyclase and, in some cases, to increases in Cai2+, but the molecular basis of signalling is unclear Mutagenesis studies of recombinant PTH/PTHrP receptors indicates that large portions of the third intracellular loop and C-terminal tail can be deleted and/or mutated without major loss of receptor-G-protein interaction, as evidenced by high affinity ligand binding and signal transduction. However, specific determinants in these domains appear to modulate the efficiency of effector activation. Further studies are needed to define the contact sites for PTH/PTHrP receptor-G-protein interaction.

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甲状旁腺激素受体及甲状旁腺激素相关蛋白的结构和功能。
甲状旁腺激素(PTH)和PTH相关蛋白(PTHrP)受体是g蛋白偶联受体亚家族的成员。该亚家族包括降钙素、分泌素、血管活性肠多肽、胰高血糖素及相关肽、生长激素释放激素和垂体腺苷酸环化酶激活肽的受体。这些受体将激动剂的占据与腺苷酸环化酶的激活结合,在某些情况下,与Cai2+的增加结合,但信号传导的分子基础尚不清楚,但重组PTH/PTHrP受体的诱变研究表明,第三胞内环和c端尾部的大部分可以被删除和/或突变,而不会导致受体- g蛋白相互作用的重大损失,这证明了高亲和力配体结合和信号转导。然而,在这些区域的特定决定因素似乎调节效应激活的效率。需要进一步的研究来确定PTH/PTHrP受体- g蛋白相互作用的接触位点。
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