血清素受体家族的结构研究

Apeksha Parajulee, Kuglae Kim
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引用次数: 0

摘要

血清素受体,也被称为5-羟色胺受体,属于G蛋白偶联受体(gpcr)超家族。它们调节血清素的作用,血清素是一种神经递质,在包括情绪调节、认知和食欲在内的一系列功能中起着关键作用。5-羟色胺的功能是由一个5-羟色胺受体家族介导的,包括12个gpcr,属于6个主要家族:5-HT1、5-HT2、5-HT4、5-HT5、5-HT6和5-HT7。尽管具有不同的特征和功能,但这些受体亚型具有共同的结构特征和信号传导机制。了解5 -羟色胺受体家族的结构、功能和药理学对于揭示5 -羟色胺信号的复杂性和开发针对神经精神疾病的靶向治疗方法至关重要。然而,开发选择性靶向特定受体亚型的药物是具有挑战性的,因为它们的正畸结合位点结构相似。本文综述了5-羟色胺受体结构研究的最新进展,重点介绍了每种亚型的关键结构特征,并揭示了它们作为精神健康和神经疾病(如抑郁症、焦虑症、精神分裂症和偏头痛)药物靶点的潜力。[BMB报告2023;56(10): 527 - 536)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural studies of serotonin receptor family
Serotonin receptors, also known as 5-HT receptors, belong to the G protein-coupled receptors (GPCRs) superfamily. They mediate the effects of serotonin, a neurotransmitter that plays a key role in a wide range of functions including mood regulation, cognition and appetite. The functions of serotonin are mediated by a family of 5-HT receptors including 12 GPCRs belonging to six major families: 5-HT1, 5-HT2, 5-HT4, 5-HT5, 5-HT6 and 5-HT7. Despite their distinct characteristics and functions, these receptors' subtypes share common structural features and signaling mechanisms. Understanding the structure, functions and pharmacology of the serotonin receptor family is essential for unraveling the complexities of serotonin signaling and developing targeted therapeutics for neuropsychiatric disorders. However, developing drugs that selectively target specific receptor subtypes is challenging due to the structural similarities in their orthosteric binding sites. This review focuses on the recent advancements in the structural studies of 5-HT receptors, highlighting the key structural features of each subtype and shedding light on their potential as targets for mental health and neurological disorders (such as depression, anxiety, schizophrenia, and migraine) drugs. [BMB Reports 2023; 56(10): 527-536].
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