Nanodomains enriched in arachidonic acid promote P2Y12 receptor oligomerization in the platelet plasma membrane

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Florentin Allemand , Semen Yesylevskyy , Jennifer Lagoutte-Renosi , Siamak Davani , Christophe Ramseyer
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Abstract

P2Y12 receptors on the platelet plasma membrane are targeted by several antiplatelets drugs. Although oligomerization and functioning of P2Y12 receptors depend on the membrane environment, little is known about their preferred membrane localization and the role of surrounding lipid composition, especially the arachidonic acids (ARA), which are abundant in platelets. Coarse-grained molecular dynamics simulations of platelet plasma membrane based on the lipidomics data were used to investigate the P2Y12 lipid environment and the involvement of ARA in its oligomerization in platelet plasma membranes. The platelet plasma membrane contains two types of lipids nanodomains: ordered, enriched in SM and cholesterol, and disordered, enriched in ARA-containing lipids. P2Y12 receptors prefer to localize in these ARA-rich domains and induce the sorting of the ARA-containing lipids in their vicinity. This ARA-rich environment promotes the oligomerization of P2Y12 receptors and stabilizes the protein-protein interfaces of oligomers. As summary, oligomerization of P2Y12 receptors is promoted in ARA-rich nano-domains of the platelet plasma membrane.

Abstract Image

富含花生四烯酸的纳米域可促进血小板质膜中 P2Y12 受体的寡聚化。
血小板浆膜上的 P2Y12 受体是多种抗血小板药物的靶点。虽然 P2Y12 受体的寡聚化和功能取决于膜环境,但人们对其首选膜定位以及周围脂质成分,尤其是血小板中含量丰富的花生四烯酸(ARA)的作用知之甚少。基于脂质组学数据的血小板质膜粗粒度分子动力学模拟被用来研究血小板质膜中 P2Y12 的脂质环境以及 ARA 在其低聚作用中的参与。血小板浆膜包含两种类型的脂质纳米域:有序的,富含SM和胆固醇;无序的,富含ARA脂质。P2Y12 受体喜欢定位在这些富含 ARA 的结构域中,并诱导其附近的含 ARA 脂质分选。这种富含 ARA 的环境促进了 P2Y12 受体的寡聚化,并稳定了寡聚体的蛋白质-蛋白质界面。综上所述,血小板质膜上富含 ARA 的纳米区促进了 P2Y12 受体的寡聚化。
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来源期刊
Biochimica et biophysica acta. Biomembranes
Biochimica et biophysica acta. Biomembranes 生物-生化与分子生物学
CiteScore
8.20
自引率
5.90%
发文量
175
审稿时长
2.3 months
期刊介绍: BBA Biomembranes has its main focus on membrane structure, function and biomolecular organization, membrane proteins, receptors, channels and anchors, fluidity and composition, model membranes and liposomes, membrane surface studies and ligand interactions, transport studies, and membrane dynamics.
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