G蛋白偶联受体
腺苷受体
受体
计算生物学
药物发现
生物
共焦显微镜
化学
腺苷
配体(生物化学)
生物化学
细胞生物学
兴奋剂
作者
Bert L. H. Beerkens,Çağla Koç,Rongfang Liu,Bogdan I. Florea,Sylvia E. Le Dévédec,Laura H. Heitman,Adriaan P. IJzerman,Daan van der Es
标识
DOI:10.1021/acschembio.2c00589
摘要
G protein-coupled receptors (GPCRs) have been known for decades as attractive drug targets. This has led to the development and approval of many ligands targeting GPCRs. Although ligand binding effects have been studied thoroughly for many GPCRs, there are multiple aspects of GPCR signaling that remain poorly understood. The reasons for this are the difficulties that are encountered upon studying GPCRs, for example, a poor solubility and low expression levels. In this work, we have managed to overcome some of these issues by developing an affinity-based probe for a prototypic GPCR, the adenosine A1 receptor (A1AR). Here, we show the design, synthesis, and biological evaluation of this probe in various biochemical assays, such as SDS-PAGE, confocal microscopy, and chemical proteomics.
科研通智能强力驱动
Strongly Powered by AbleSci AI