化学
共价键
组合化学
配体(生物化学)
体内
药物发现
膜
体外
色谱法
化学合成
受体
生物化学
有机化学
生物技术
生物
作者
Zhaomin Xia,Qiumei Zhu,Yi Shan,Jiayu Lu,M. An,Xiaoxue Mo,Siqi Wang,Wen‐Bin Yang,Qian Hua,Huaizhen He,Chéng Wáng
标识
DOI:10.1021/acs.jmedchem.5c00258
摘要
Mas-related G protein-coupled receptor X2 (MrgX2) plays a key role in pseudoallergy reactions; thus, it is of great significance to screen compounds with antipseudoallergy activity via MrgX2. Cell membrane chromatography (CMC) demonstrates great potential in drug screening, but it requires further optimization to improve its specificity and stability. In this study, a new CMC system incorporating His-tag-oriented immobilized proteins was constructed to screen MrgX2 antagonists. Single His-tag-fused MrgX2 was extracted intactly and covalently bond to divinyl sulfone-modified amino silica gel to obtain bioaffinity composites. The characterized composites were utilized to establish a MrgX2-His-tag@VS/CMC system to screen MrgX2 antagonists. Compound Z-3578 was screened from a G protein-coupled receptor compound library of 3010 compounds and revealed its efficient antipseudoallergy activity in vitro and in vivo via MrgX2. In conclusion, the new oriented-immobilized CMC system will provide an efficient analytical tool for screening active precursors.
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