化学
四肽
G蛋白偶联受体
受体
配体(生物化学)
兴奋剂
组合化学
立体化学
鉴定(生物学)
计算生物学
分辨率(逻辑)
多巴胺
分子模型
多巴胺受体
连接器
折叠(DSP实现)
寡肽
生物物理学
联轴节(管道)
药物发现
生物化学
基质(化学分析)
HEK 293细胞
作者
Hongyu Wen,Zhisheng Lai,Jinhui Wang,Minhui Shen,Xiaoru Peng,Wei Lin,Wei Ting Xia,Yu‐Xin Ye,Jianqiao Xu,Gangfeng Ouyang
标识
DOI:10.1021/acs.analchem.5c04692
摘要
G protein-coupled receptors (GPCRs) are targets for 36% approved drugs. However, identifying GPCR ligands remains cumbersome owing to their inherent instability and inevitably associated salts and detergents. Here, we resolve these bottlenecks by developing a stereoselective cyclic tetrapeptide (CP1) for identifying dopamine (DA) receptor ligands from complex matrices. This innovative strategy enables online coupling with liquid chromatography to reduce matrix complexity and accurate identification of putative ligands based on the high mass spectral resolution combined with the predictable pronounced mass-to-charge ratio shifts. CP1 is revealed to recognize the shared scaffolds or catecholic groups of the ligands, which is further proven tunable via conformational or submolecular modifications. Thereby, the first identification of β-phenylethylamine (β-PEA, an agonist of DA receptors) in underground water and the identification of 1-phenylguanidine (PG) and 1,3-diphenylguanidine (DPG) as antagonists of DA receptor D1 (DRD1) are achieved, raising concerns about their potential unintended effects on human dopamine receptors. This study demonstrates oligopeptides as a transformative class of gas-phase molecular tools for GPCR ligand discovery, effectively overcoming bottlenecks of conventional receptor-based methodologies.
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