Department of Biosensorics, Institute of Physiology, Universität Hohenheim, 70599 Stuttgart, Germany.
Cells. 2014 Apr 8;3(2):258-87. doi: 10.3390/cells3020258.
Transient receptor potential (TRP) channels constitute an ancient family of cation channels that have been found in many eukaryotic organisms from yeast to human. TRP channels exert a multitude of physiological functions ranging from Ca2+ homeostasis in the kidney to pain reception and vision. These channels are activated by a wide range of stimuli and undergo covalent post-translational modifications that affect and modulate their subcellular targeting, their biophysical properties, or channel gating. These modifications include N-linked glycosylation, protein phosphorylation, and covalent attachment of chemicals that reversibly bind to specific cysteine residues. The latter modification represents an unusual activation mechanism of ligand-gated ion channels that is in contrast to the lock-and-key paradigm of receptor activation by its agonists. In this review, we summarize the post-translational modifications identified on TRP channels and, when available, explain their physiological role.
瞬时受体电位 (TRP) 通道构成了一个古老的阳离子通道家族,在从酵母到人等许多真核生物中都有发现。TRP 通道发挥着多种生理功能,从肾脏中的 Ca2+稳态到疼痛感知和视觉。这些通道由多种刺激激活,并经历影响和调节其亚细胞靶向、生物物理特性或通道门控的共价翻译后修饰。这些修饰包括 N-连接糖基化、蛋白质磷酸化以及与可逆结合到特定半胱氨酸残基的化学物质的共价连接。后一种修饰代表了一种不寻常的配体门控离子通道激活机制,与激动剂通过其受体的“锁钥”范例激活受体形成对比。在这篇综述中,我们总结了在 TRP 通道上鉴定到的翻译后修饰,并在有可用信息的情况下解释了它们的生理作用。