Suppr超能文献

受体异源二聚化与药物发现。

Receptor heteromerization and drug discovery.

机构信息

Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY10029, USA.

出版信息

Trends Pharmacol Sci. 2010 Mar;31(3):124-30. doi: 10.1016/j.tips.2009.11.008. Epub 2010 Jan 7.

Abstract

G-protein-coupled receptors (GPCRs) are membrane proteins that convert extracellular information into intracellular signals. They are involved in many biological processes and therefore represent powerful targets to modulate physiological and pathological states. Recent studies have demonstrated that GPCR activity is regulated by several mechanisms. Among these, protein-protein interactions (and in particular interactions with other receptors leading to heteromerization) has been shown to have an important role in modulating GPCR function. This has expanded their repertoire of signaling and added a new level of regulation to their physiological roles. Emerging studies provide evidence for tissue-specific and disease-specific receptor heteromerization. This suggests that heteromers represent novel drug targets for the identification of selective compounds with potentially fewer side-effects.

摘要

G 蛋白偶联受体(GPCRs)是一种将细胞外信息转化为细胞内信号的膜蛋白。它们参与许多生物过程,因此是调节生理和病理状态的有力靶点。最近的研究表明,GPCR 活性受到多种机制的调节。在这些机制中,蛋白质-蛋白质相互作用(特别是与其他受体的相互作用导致异源二聚化)已被证明在调节 GPCR 功能方面发挥着重要作用。这扩展了它们的信号转导谱,并为其生理作用增加了新的调节层次。新兴的研究为组织特异性和疾病特异性受体异源二聚体提供了证据。这表明,异源二聚体代表了新型药物靶点,用于鉴定潜在副作用更少的选择性化合物。

相似文献

1
Receptor heteromerization and drug discovery.受体异源二聚化与药物发现。
Trends Pharmacol Sci. 2010 Mar;31(3):124-30. doi: 10.1016/j.tips.2009.11.008. Epub 2010 Jan 7.
3
G Protein-Coupled Receptor Heteromers.G蛋白偶联受体异聚体
Annu Rev Pharmacol Toxicol. 2016;56:403-25. doi: 10.1146/annurev-pharmtox-011613-135952. Epub 2015 Oct 22.
7
Oligomerization of GPCRs involved in endocrine regulation.参与内分泌调节的G蛋白偶联受体的寡聚化。
J Mol Endocrinol. 2016 Jul;57(1):R59-80. doi: 10.1530/JME-16-0049. Epub 2016 May 5.
8
Contribution of heteromerization to G protein-coupled receptor function.异源二聚化对G蛋白偶联受体功能的贡献。
Curr Opin Pharmacol. 2017 Feb;32:23-31. doi: 10.1016/j.coph.2016.10.006. Epub 2016 Nov 9.
9
G-protein coupled receptors: advances in simulation and drug discovery.G蛋白偶联受体:模拟与药物发现的进展
Curr Opin Struct Biol. 2016 Dec;41:83-89. doi: 10.1016/j.sbi.2016.06.008. Epub 2016 Jun 22.

引用本文的文献

4
Is the Neuropeptide PEN a Ligand of GPR83?神经肽 PEN 是否为 GPR83 的配体?
Int J Mol Sci. 2023 Oct 12;24(20):15117. doi: 10.3390/ijms242015117.
7
Heterobivalent Ligand for the Adenosine A-Dopamine D Receptor Heteromer.双价配体与腺苷 A-多巴胺 D 受体异源二聚体。
J Med Chem. 2022 Jan 13;65(1):616-632. doi: 10.1021/acs.jmedchem.1c01763. Epub 2022 Jan 4.
9
Modulation of endothelium function by fatty acids.脂肪酸对血管内皮功能的调节。
Mol Cell Biochem. 2022 Jan;477(1):15-38. doi: 10.1007/s11010-021-04260-9. Epub 2021 Sep 16.
10
Engineering G-quadruplex aptamer to modulate its binding specificity.工程化G-四链体适体以调节其结合特异性。
Natl Sci Rev. 2020 Aug 31;8(4):nwaa202. doi: 10.1093/nsr/nwaa202. eCollection 2021 Apr.

本文引用的文献

4
Cell surface targeting of mu-delta opioid receptor heterodimers by RTP4.RTP4介导的μ-δ阿片受体异二聚体的细胞表面靶向作用
Proc Natl Acad Sci U S A. 2008 Oct 14;105(41):16045-50. doi: 10.1073/pnas.0804106105. Epub 2008 Oct 3.
8
Receptor pair for schizophrenia.精神分裂症的受体对。
Pediatr Res. 2008 Jul;64(1):1. doi: 10.1203/PDR.0b013e318180052a.
9
The endocannabinoid system in obesity and type 2 diabetes.肥胖症和2型糖尿病中的内源性大麻素系统。
Diabetologia. 2008 Aug;51(8):1356-67. doi: 10.1007/s00125-008-1048-2. Epub 2008 Jun 18.

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