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五聚体配体门控离子通道的脂质结合与脂质调节的最新见解

Recent Insight into Lipid Binding and Lipid Modulation of Pentameric Ligand-Gated Ion Channels.

作者信息

Ananchenko Anna, Hussein Toka O K, Mody Deepansh, Thompson Mackenzie J, Baenziger John E

机构信息

Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, 451 Smyth Road, Ottawa, ON K1H 8M5, Canada.

出版信息

Biomolecules. 2022 Jun 10;12(6):814. doi: 10.3390/biom12060814.

DOI:10.3390/biom12060814
PMID:35740939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9221113/
Abstract

Pentameric ligand-gated ion channels (pLGICs) play a leading role in synaptic communication, are implicated in a variety of neurological processes, and are important targets for the treatment of neurological and neuromuscular disorders. Endogenous lipids and lipophilic compounds are potent modulators of pLGIC function and may help shape synaptic communication. Increasing structural and biophysical data reveal sites for lipid binding to pLGICs. Here, we update our evolving understanding of pLGIC-lipid interactions highlighting newly identified modes of lipid binding along with the mechanistic understanding derived from the new structural data.

摘要

五聚体配体门控离子通道(pLGICs)在突触通讯中起主导作用,涉及多种神经学过程,并且是治疗神经和神经肌肉疾病的重要靶点。内源性脂质和亲脂性化合物是pLGIC功能的有效调节剂,可能有助于塑造突触通讯。越来越多的结构和生物物理数据揭示了脂质与pLGICs结合的位点。在这里,我们更新了对pLGIC-脂质相互作用的不断发展的理解,突出了新发现的脂质结合模式以及从新结构数据中获得的机制理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/5588a5bedbf1/biomolecules-12-00814-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/8f871a327d3b/biomolecules-12-00814-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/722315c8117c/biomolecules-12-00814-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/5bef79e844b7/biomolecules-12-00814-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/7f09996f4ee4/biomolecules-12-00814-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/ea54d1eee3c3/biomolecules-12-00814-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/5588a5bedbf1/biomolecules-12-00814-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/8f871a327d3b/biomolecules-12-00814-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/722315c8117c/biomolecules-12-00814-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/5bef79e844b7/biomolecules-12-00814-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/7f09996f4ee4/biomolecules-12-00814-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/ea54d1eee3c3/biomolecules-12-00814-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fa/9221113/5588a5bedbf1/biomolecules-12-00814-g006.jpg

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本文引用的文献

1
Differential assembly diversifies GABA receptor structures and signalling.差异组装使 GABA 受体结构和信号多样化。
Nature. 2022 Apr;604(7904):190-194. doi: 10.1038/s41586-022-04517-3. Epub 2022 Mar 30.
2
Structural mechanism of muscle nicotinic receptor desensitization and block by curare.肌肉烟碱型受体脱敏和阻断的结构机制 由箭毒引起。
Nat Struct Mol Biol. 2022 Apr;29(4):386-394. doi: 10.1038/s41594-022-00737-3. Epub 2022 Mar 17.
3
Mechanisms of inhibition and activation of extrasynaptic αβ GABA receptors.αβ 型 GABA 受体的抑制和激活机制。
胆固醇和阴离子脂质与肌肉型 Torpedo 乙酰胆碱受体的状态依赖结合。
Commun Biol. 2024 Apr 10;7(1):437. doi: 10.1038/s42003-024-06106-8.
4
Conformational trajectory of allosteric gating of the human cone photoreceptor cyclic nucleotide-gated channel.变构门控的人锥形光感受器环核苷酸门控通道的构象轨迹。
Nat Commun. 2023 Jul 18;14(1):4284. doi: 10.1038/s41467-023-39971-8.
5
Studying Membrane Protein-Lipid Specificity through Direct Native Mass Spectrometric Analysis from Tunable Proteoliposomes.通过可调谐的蛋白脂囊泡的直接天然质谱分析研究膜蛋白-脂质特异性。
J Am Soc Mass Spectrom. 2023 Sep 6;34(9):1917-1927. doi: 10.1021/jasms.3c00110. Epub 2023 Jul 11.
6
Multiscale molecular dynamics simulations predict arachidonic acid binding sites in human ASIC1a and ASIC3 transmembrane domains.多尺度分子动力学模拟预测人类 ASIC1a 和 ASIC3 跨膜域中花生四烯酸结合位点。
J Gen Physiol. 2023 Mar 6;155(3). doi: 10.1085/jgp.202213259. Epub 2023 Jan 10.
7
Open-channel structure of a pentameric ligand-gated ion channel reveals a mechanism of leaflet-specific phospholipid modulation.五聚体配体门控离子通道的开放式结构揭示了小叶特异性磷脂调制的机制。
Nat Commun. 2022 Nov 17;13(1):7017. doi: 10.1038/s41467-022-34813-5.
Nature. 2022 Feb;602(7897):529-533. doi: 10.1038/s41586-022-04402-z. Epub 2022 Feb 9.
4
Conformational transitions and ligand-binding to a muscle-type nicotinic acetylcholine receptor.构象转变与配体对肌肉型烟碱型乙酰胆碱受体的结合
Neuron. 2022 Apr 20;110(8):1358-1370.e5. doi: 10.1016/j.neuron.2022.01.013. Epub 2022 Feb 8.
5
Druggable Lipid Binding Sites in Pentameric Ligand-Gated Ion Channels and Transient Receptor Potential Channels.五聚体配体门控离子通道和瞬时受体电位通道中的可药物靶向脂质结合位点
Front Physiol. 2022 Jan 4;12:798102. doi: 10.3389/fphys.2021.798102. eCollection 2021.
6
Polyunsaturated fatty acids inhibit a pentameric ligand-gated ion channel through one of two binding sites.多不饱和脂肪酸通过两个结合位点之一抑制五聚体配体门控离子通道。
Elife. 2022 Jan 4;11:e74306. doi: 10.7554/eLife.74306.
7
Probing the molecular basis for signal transduction through the Zinc-Activated Channel (ZAC).探究锌激活通道(ZAC)信号转导的分子基础。
Biochem Pharmacol. 2021 Nov;193:114781. doi: 10.1016/j.bcp.2021.114781. Epub 2021 Sep 21.
8
Architecture and assembly mechanism of native glycine receptors.天然甘氨酸受体的结构与组装机制。
Nature. 2021 Nov;599(7885):513-517. doi: 10.1038/s41586-021-04022-z. Epub 2021 Sep 23.
9
Characterization of the subunit composition and structure of adult human glycine receptors.成人甘氨酸受体亚基组成与结构的特征。
Neuron. 2021 Sep 1;109(17):2707-2716.e6. doi: 10.1016/j.neuron.2021.08.019.
10
Protein-lipid interplay at the neuromuscular junction.神经肌肉接头处的蛋白质-脂质相互作用。
Microscopy (Oxf). 2022 Feb 18;71(Supplement_1):i66-i71. doi: 10.1093/jmicro/dfab023.