• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

拼凑拼图碎片:磷脂- G蛋白偶联受体相互作用的当前原子水平图景

Integrating the puzzle pieces: the current atomistic picture of phospholipid-G protein coupled receptor interactions.

作者信息

Parrill Abby L, Tigyi Gabor

机构信息

Department of Chemistry, The University of Memphis, Memphis, TN 38152, USA.

出版信息

Biochim Biophys Acta. 2013 Jan;1831(1):2-12. doi: 10.1016/j.bbalip.2012.09.002. Epub 2012 Sep 12.

DOI:10.1016/j.bbalip.2012.09.002
PMID:22982815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3591812/
Abstract

A compelling question of how phospholipids interact with their target receptors has been of interest since the first receptor-mediated effects were reported. The recent report of a crystal structure for the S1P(1) receptor in complex with an antagonist phospholipid provides interesting perspective on the insights that had previously been gained through structure-activity studies of the phospholipids, as well as modeling and mutagenesis studies of the receptors. This review integrates these varied lines of investigation in the context of their various contributions to our current understanding of phospholipid-receptor interactions. This article is part of a Special Issue entitled Advances in Lysophospholipid Research.

摘要

自首次报道受体介导的效应以来,磷脂如何与其靶受体相互作用这一引人关注的问题一直备受关注。最近关于S1P(1)受体与拮抗剂磷脂复合物晶体结构的报道,为先前通过磷脂构效关系研究以及受体建模和诱变研究获得的见解提供了有趣的视角。本综述在它们对我们目前对磷脂 - 受体相互作用理解的各种贡献的背景下,整合了这些不同的研究方向。本文是名为《溶血磷脂研究进展》特刊的一部分。

相似文献

1
Integrating the puzzle pieces: the current atomistic picture of phospholipid-G protein coupled receptor interactions.拼凑拼图碎片:磷脂- G蛋白偶联受体相互作用的当前原子水平图景
Biochim Biophys Acta. 2013 Jan;1831(1):2-12. doi: 10.1016/j.bbalip.2012.09.002. Epub 2012 Sep 12.
2
Novel clusters of receptors for sphingosine-1-phosphate, sphingosylphosphorylcholine, and (lyso)-phosphatidic acid: new receptors for "old" ligands.鞘氨醇-1-磷酸、鞘氨醇磷酰胆碱和(溶血)磷脂酸的新型受体簇:“旧”配体的新受体。
J Cell Biochem. 2004 Aug 1;92(5):923-36. doi: 10.1002/jcb.20092.
3
Molecular recognition in the sphingosine 1-phosphate receptor family.1-磷酸鞘氨醇受体家族中的分子识别
J Mol Graph Model. 2008 Jun;26(8):1189-201. doi: 10.1016/j.jmgm.2007.11.001. Epub 2007 Nov 17.
4
Cell surface receptors in lysophospholipid signaling.溶血磷脂信号传导中的细胞表面受体。
Semin Cell Dev Biol. 2004 Oct;15(5):457-65. doi: 10.1016/j.semcdb.2004.05.005.
5
Homo- and hetero-dimerization of LPA/S1P receptors, OGR1 and GPR4.溶血磷脂酸/鞘氨醇-1-磷酸受体、OGR1和GPR4的同源和异源二聚化。
Biochim Biophys Acta. 2006 Oct;1761(10):1200-12. doi: 10.1016/j.bbalip.2006.08.011. Epub 2006 Aug 30.
6
LPA(3), a unique G protein-coupled receptor for lysophosphatidic acid.LPA(3),溶血磷脂酸的独特 G 蛋白偶联受体。
Prog Lipid Res. 2010 Oct;49(4):335-42. doi: 10.1016/j.plipres.2010.03.001. Epub 2010 Mar 15.
7
Sphingosine 1-phosphate and lysophosphatidic acid receptors: agonist and antagonist binding and progress toward development of receptor-specific ligands.鞘氨醇-1-磷酸和溶血磷脂酸受体:激动剂与拮抗剂结合以及受体特异性配体开发的进展
Semin Cell Dev Biol. 2004 Oct;15(5):467-76. doi: 10.1016/j.semcdb.2004.05.006.
8
A single amino acid determines preference between phospholipids and reveals length restriction for activation of the S1P4 receptor.单个氨基酸决定了对磷脂的偏好,并揭示了S1P4受体激活的长度限制。
BMC Biochem. 2004 Aug 6;5:12. doi: 10.1186/1471-2091-5-12.
9
Lysophosphatidic acid (LPA) receptors: signaling properties and disease relevance.溶血磷脂酸(LPA)受体:信号特性与疾病相关性。
Prostaglandins Other Lipid Mediat. 2010 Apr;91(3-4):130-8. doi: 10.1016/j.prostaglandins.2009.02.002. Epub 2009 Mar 4.
10
Signal transduction responses to lysophosphatidic acid and sphingosine 1-phosphate in human prostate cancer cells.人前列腺癌细胞中对溶血磷脂酸和1-磷酸鞘氨醇的信号转导反应。
Prostate. 2009 Oct 1;69(14):1493-506. doi: 10.1002/pros.20994.

引用本文的文献

1
Lysophosphatidic acid (LPA) as a modulator of plasma membrane Ca-ATPase from basolateral membranes of kidney proximal tubules.溶血磷脂酸(LPA)作为肾脏近端小管基底外侧膜质膜 Ca-ATP 酶的调节剂。
J Physiol Biochem. 2021 May;77(2):321-329. doi: 10.1007/s13105-021-00800-5. Epub 2021 Mar 11.
2
Lipid-Protein Interactions Are a Unique Property and Defining Feature of G Protein-Coupled Receptors.脂质-蛋白相互作用是 G 蛋白偶联受体的独特性质和定义特征。
Biophys J. 2020 Apr 21;118(8):1887-1900. doi: 10.1016/j.bpj.2020.03.008. Epub 2020 Mar 20.
3
A Novel Agonist of the Type 1 Lysophosphatidic Acid Receptor (LPA), UCM-05194, Shows Efficacy in Neuropathic Pain Amelioration.新型 1 型溶血磷脂酸受体(LPA)激动剂 UCM-05194 可有效改善神经病理性疼痛。
J Med Chem. 2020 Mar 12;63(5):2372-2390. doi: 10.1021/acs.jmedchem.9b01287. Epub 2019 Dec 16.
4
Emerging Diversity in Lipid-Protein Interactions.脂质-蛋白质相互作用的新多样性。
Chem Rev. 2019 May 8;119(9):5775-5848. doi: 10.1021/acs.chemrev.8b00451. Epub 2019 Feb 13.
5
Lysophosphatidic acid type 2 receptor agonists in targeted drug development offer broad therapeutic potential.溶血磷脂酸 2 型受体激动剂在靶向药物研发中具有广阔的治疗潜力。
J Lipid Res. 2019 Mar;60(3):464-474. doi: 10.1194/jlr.S091744. Epub 2019 Jan 28.
6
Molecular mechanisms of target recognition by lipid GPCRs: relevance for cancer.脂质G蛋白偶联受体的靶点识别分子机制:与癌症的相关性
Oncogene. 2016 Aug 4;35(31):4021-35. doi: 10.1038/onc.2015.467. Epub 2015 Dec 7.
7
The Bulk of Autotaxin Activity Is Dispensable for Adult Mouse Life.自分泌运动因子的大部分活性对于成年小鼠的生命并非必需。
PLoS One. 2015 Nov 16;10(11):e0143083. doi: 10.1371/journal.pone.0143083. eCollection 2015.
8
Generic GPCR residue numbers - aligning topology maps while minding the gaps.通用GPCR残基编号——在留意缺口的同时对齐拓扑图。
Trends Pharmacol Sci. 2015 Jan;36(1):22-31. doi: 10.1016/j.tips.2014.11.001. Epub 2014 Dec 22.
9
Structural Characterization of an LPA1 Second Extracellular Loop Mimetic with a Self-Assembling Coiled-Coil Folding Constraint.具有自组装卷曲螺旋折叠约束的 LPA1 第二细胞外环类似物的结构特征。
Int J Mol Sci. 2013 Jan 29;14(2):2788-807. doi: 10.3390/ijms14022788.

本文引用的文献

1
Optimization of a Potent, Orally Active S1P1 Agonist Containing a Quinolinone Core.含喹啉酮核心的强效口服活性S1P1激动剂的优化
ACS Med Chem Lett. 2011 Nov 23;3(1):74-8. doi: 10.1021/ml200252b. eCollection 2012 Jan 12.
2
Discovery of a Selective S1P1 Receptor Agonist Efficacious at Low Oral Dose and Devoid of Effects on Heart Rate.发现一种低口服剂量有效且对心率无影响的选择性S1P1受体激动剂。
ACS Med Chem Lett. 2011 Mar 24;2(6):444-9. doi: 10.1021/ml2000214. eCollection 2011 Jun 9.
3
Discovery of AMG 369, a Thiazolo[5,4-b]pyridine Agonist of S1P1 and S1P5.AMG 369的发现,一种噻唑并[5,4-b]吡啶类S1P1和S1P5激动剂。
ACS Med Chem Lett. 2010 Dec 29;2(2):107-12. doi: 10.1021/ml100306h. eCollection 2011 Feb 10.
4
Benzofuran Derivatives as Potent, Orally Active S1P1 Receptor Agonists: A Preclinical Lead Molecule for MS.苯并呋喃衍生物作为强效、口服活性的S1P1受体激动剂:一种用于多发性硬化症的临床前先导分子。
ACS Med Chem Lett. 2010 Nov 9;2(2):97-101. doi: 10.1021/ml100227q. eCollection 2011 Feb 10.
5
4-Methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide: A Potent and Selective Agonist of S1P1.4-甲氧基-N-[2-(三氟甲基)联苯-4-基甲酰基]烟酰胺:一种强效且选择性的S1P1激动剂。
ACS Med Chem Lett. 2011 Jul 29;2(10):752-7. doi: 10.1021/ml2001399. eCollection 2011 Oct 13.
6
Structure of the first sphingosine 1-phosphate receptor.首个神经酰胺 1-磷酸受体结构。
Sci Signal. 2012 May 22;5(225):pe23. doi: 10.1126/scisignal.2003160.
7
Crystal structure of a lipid G protein-coupled receptor.脂质 G 蛋白偶联受体的晶体结构。
Science. 2012 Feb 17;335(6070):851-5. doi: 10.1126/science.1215904.
8
Discovery of CS-2100, a potent, orally active and S1P3-sparing S1P1 agonist.发现 CS-2100,一种强效、口服活性且 S1P3 节约型 S1P1 激动剂。
Bioorg Med Chem Lett. 2012 Feb 15;22(4):1788-92. doi: 10.1016/j.bmcl.2011.12.019. Epub 2012 Jan 2.
9
Structure-activity relationship studies of S1P agonists with a dihydronaphthalene scaffold.具有二氢萘骨架的 S1P 激动剂的构效关系研究。
Bioorg Med Chem Lett. 2012 Jan 1;22(1):144-8. doi: 10.1016/j.bmcl.2011.11.048. Epub 2011 Nov 20.
10
Novel immunomodulators based on an oxazolin-2-one-4-carboxamide scaffold.基于噁唑啉-2-酮-4-甲酰胺支架的新型免疫调节剂。
Bioorg Med Chem Lett. 2012 Jan 1;22(1):553-7. doi: 10.1016/j.bmcl.2011.10.088. Epub 2011 Nov 6.