药物发现
神经科学
功能多样性
功能(生物学)
计算生物学
受体
结构功能
多样性(政治)
分子药理学
兴奋剂
生物
医学
药理学
生物信息学
遗传学
生态学
物理
粒子物理学
社会学
人类学
标识
DOI:10.1016/j.tips.2023.02.002
摘要
Mas-related G protein-coupled receptor (MRGPR) family members play important roles in the sensation of noxious stimuli and represent novel targets for the treatment of itch and pain. MRGPRs recognize a diversity of agonists and display complicated downstream signaling profiles, high sequence diversity across species, and many polymorphisms in humans. The recent structural advances on MRGPRs reveal unique structural features and diverse agonist recognition modes of this receptor family, which should facilitate the structure-based drug discovery at MRGPRs. In addition, the newly discovered ligands also provide valuable tools to explore the function and the therapeutic potential of MRGPRs. In this review, we discuss these progresses in our understanding of MRGPRs and highlight the challenges and potential opportunities for the future drug discovery at these receptors.
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