Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom; email:
Annu Rev Pharmacol Toxicol. 2020 Jan 6;60:31-50. doi: 10.1146/annurev-pharmtox-010919-023411. Epub 2019 Sep 10.
Ion channels and G protein-coupled receptors (GPCRs) are regulated by lipids in their membrane environment. Structural studies combined with biophysical and molecular simulation investigations reveal interaction sites for specific lipids on membrane protein structures. For K channels, PIP plays a key role in regulating Kv and Kir channels. Likewise, several recent cryo-EM structures of TRP channels have revealed bound lipids, including PIP and cholesterol. Among the pentameric ligand-gated ion channel family, structural and biophysical studies suggest the M4 TM helix may act as a lipid sensor, e.g., forming part of the binding sites for neurosteroids on the GABA receptor. Structures of GPCRs have revealed multiple cholesterol sites, which may modulate both receptor dynamics and receptor oligomerization. PIP also interacts with GPCRs and may modulate their interactions with G proteins. Overall, it is evident that multiple lipid binding sites exist on channels and receptors that modulate their function allosterically and are potential druggable sites.
离子通道和 G 蛋白偶联受体 (GPCR) 受其膜环境中脂质的调节。结构研究与生物物理和分子模拟研究相结合,揭示了特定脂质在膜蛋白结构上的相互作用位点。对于 K 通道,PIP 在调节 Kv 和 Kir 通道方面起着关键作用。同样,最近几项关于 TRP 通道的冷冻电镜结构揭示了结合的脂质,包括 PIP 和胆固醇。在五聚体配体门控离子通道家族中,结构和生物物理研究表明 M4 TM 螺旋可能充当脂质传感器,例如,形成 GABA 受体上神经甾体结合位点的一部分。GPCR 的结构揭示了多个胆固醇结合位点,这些位点可能调节受体的动力学和受体寡聚化。PIP 还与 GPCR 相互作用,并可能调节它们与 G 蛋白的相互作用。总的来说,显然在通道和受体上存在多个调节其变构功能的脂质结合位点,这些位点可能是潜在的可成药位点。