The Role of Lipids in Allosteric Modulation of Dopamine D2 Receptor-In Silico Study

被引:5
|
作者
Zuk, Justyna [1 ]
Bartuzi, Damian [1 ]
Miszta, Przemyslaw [2 ]
Kaczor, Agnieszka A. [1 ,3 ]
机构
[1] Fac Pharm, Dept Synth & Chem Technol Pharmaceut Subst, Comp Modelling Lab, 4A Chodzki St, PL-20093 Lublin, Poland
[2] Univ Warsaw, Fac Chem, Chem Res Ctr, Biol, PL-02093 Warsaw, Poland
[3] Univ Eastern Finland, Sch Pharm, Yliopistonranta 1,POB 1627, FI-70211 Kuopio, Finland
来源
MOLECULES | 2022年 / 27卷 / 04期
关键词
allosteric modulators; dopamine D-2L receptor; GPCRs; lipid rafts; molecular dynamics; PROTEIN-COUPLED-RECEPTORS; RAFTS; CHOLESTEROL; DYNAMICS; COMPONENTS; BILAYERS; ORDER; NMR;
D O I
10.3390/molecules27041335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The dopamine D-2 receptor, belonging to the class A G protein-coupled receptors (GPCRs), is an important drug target for several diseases, including schizophrenia and Parkinson's disease. The D-2 receptor can be activated by the natural neurotransmitter dopamine or by synthetic ligands, which in both cases leads to the receptor coupling with a G protein. In addition to receptor modulation by orthosteric or allosteric ligands, it has been shown that lipids may affect the behaviour of membrane proteins. We constructed a model of a D-2 receptor with a long intracellular loop (ICL3) coupled with G(i alpha 1) or G(i alpha 2) proteins, embedded in a complex asymmetric membrane, and simulated it in complex with positive, negative or neutral allosteric ligands. In this study, we focused on the influence of ligand binding and G protein coupling on the membrane-receptor interactions. We show that there is a noticeable interplay between the cell membrane, G proteins, D-2 receptor and its modulators.
引用
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页数:14
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