编码药物作用的胃饥饿素受体的结构和功能

Yuki Shiimura, Dohyun Im, Ryosuke Tany, Hidetsugu Asada, Ryoji Kise, Eon Kurumiya, Hideko Wakasugi-Masuho, Satoshi Yasuda, Kazuma Matsui, Jun-ichi Kishikawa, Takayuki Kato, Takeshi Murata, Masayasu Kojima, So Iwata, Ikuo Masuho
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引用次数: 0

摘要

以胃饥饿素受体为靶点的药物在治疗厌食症、肥胖症和糖尿病方面具有潜力。然而,开发有效的药物是具有挑战性的。为了在广泛的药物靶点上解决这一常见问题,本研究旨在了解anamorelin(唯一被批准的靶向胃饥饿素受体的药物)与其他合成药物相比是如何起作用的。我们的研究阐明了anamorelin和miniGq受体的结构,揭示了anamorelin的超激动作用。我们证明了具有不同化学结构的配体独特地与受体结合,导致不同的构象和偏倚的信号转导。此外,我们的研究展示了结构信息在有效识别改变药物作用和导致严重功能缺陷的自然遗传变异方面的效用,为根据个体基因组序列选择正确的药物提供了基础。因此,在结构分析的基础上,本研究通过有效地利用信号偏倚和遗传变异,增强了选择靶向胃饥饿素受体的治疗药物的基础框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The structure and function of the ghrelin receptor coding for drug actions

Drugs targeting the ghrelin receptor hold therapeutic potential in anorexia, obesity and diabetes. However, developing effective drugs is challenging. To tackle this common issue across a broad drug target, this study aims to understand how anamorelin, the only approved drug targeting the ghrelin receptor, operates compared to other synthetic drugs. Our research elucidated the receptor’s structure with anamorelin and miniGq, unveiling anamorelin’s superagonistic activity. We demonstrated that ligands with distinct chemical structures uniquely bind to the receptor, resulting in diverse conformations and biasing signal transduction. Moreover, our study showcased the utility of structural information in effectively identifying natural genetic variations altering drug action and causing severe functional deficiencies, offering a basis for selecting the right medication on the basis of the individual’s genomic sequence. Thus, by building on structural analysis, this study enhances the foundational framework for selecting therapeutic agents targeting the ghrelin receptor, by effectively leveraging signaling bias and genetic variations.

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