Heuninck Joyce, Hounsou Candide, Dupuis Elodie, Trinquet Eric, Mouillac Bernard, Pin Jean-Philippe, Bonnet Dominique, Durroux Thierry
CNRS, UMR 5203, Institut de Génomique Fonctionnelle, Montpellier, France.
INSERM, U. 1191, Montpellier, France.
Methods Mol Biol. 2019;1947:151-168. doi: 10.1007/978-1-4939-9121-1_8.
Although G protein-coupled receptor (GPCR) oligomerization is a matter of debate, it has been shown that the nature of the GPCR partners within the oligomers can influence the pharmacological properties of the receptors. Therefore, finding specific ligands for homo- or hetero-oligomers opens new perspectives for drug discovery. However, no efficient experimental strategy to screen for such ligands existed yet. Indeed, conventional binding strategies do not discriminate ligand binding on GPCR monomers, homo- or hetero-oligomers. To address this issue, we recently developed a new assay based on a time-resolved FRET method that is easy to implement and that can focus on ligand binding specifically on the hetero-oligomer.
尽管G蛋白偶联受体(GPCR)的寡聚化仍存在争议,但已有研究表明,寡聚体内GPCR伙伴的性质可影响受体的药理学特性。因此,寻找同型或异型寡聚体的特异性配体为药物研发开辟了新的前景。然而,目前尚无有效的实验策略来筛选此类配体。实际上,传统的结合策略无法区分配体与GPCR单体、同型或异型寡聚体的结合。为解决这一问题,我们最近开发了一种基于时间分辨荧光共振能量转移(FRET)方法的新检测方法,该方法易于实施,且能够专注于配体与异型寡聚体的特异性结合。