神经激肽-1受体:结构动力学和信号传导

F. D. Rodríguez, R. Coveñas
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引用次数: 4

摘要

P物质(Substance P, SP)是第一个分离到的神经肽,属于速激肽家族,是神经激肽-1受体(neurokinin-1 receptor, NK-1R)的天然配体,也被称为SP受体。非肽在与蛋白质特异性结合后激活受体,并触发细胞内信号,导致不同的生化事件和随后的生理反应。本研究综述了该受体的主要结构特征,与天然和合成配体的相互作用,以及与配体和效应G蛋白相互作用后的功能构象状态。通过对NK-1受体激活所开启的主要细胞内信号通路的分析,揭示了支持代谢变化以及遗传和表观遗传调控的不同蛋白质的参与。此外,对SP在生理病理中的作用的基础和临床研究中,受体占用和受体下调和内化的分析是一个复杂而值得重视的领域。对NK-1R结构动力学的深入了解可能有助于开发和检测新的选择性合成非肽拮抗剂,作为应用于各种病理和症状的潜在治疗剂。
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The Neurokinin-1 Receptor: Structure Dynamics and Signaling
Substance P (SP), the first isolated neuropeptide, belongs to the family of tachykinin peptides and is the natural ligand of neurokinin-1 receptors (NK-1R), also named SP receptors. The undecapeptide activates the receptor after specifically binding to the protein and triggers intracellular signals leading to different biochemical events and subsequent physiological responses. This study reviews the main architectural features of this receptor, its interaction with natural and synthetic ligands, and the functional conformational states adopted after interacting with ligands and effector G proteins. The analysis of the main intracellular signaling pathways turned on by the activation of NK-1 receptors reveals the participation of different proteins supporting metabolic changes and genetic and epigenetic regulations. Furthermore, the analysis of receptor occupancy and receptor downregulation and internalization represents a complex and estimable field for basic and clinical research focused on the role of SP in physiopathology. Profound knowledge of the structural dynamics of NK-1R may help develop and assay new selective synthetic non-peptide antagonists as potential therapeutic agents applied to various pathologies and symptoms.
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