苯丙素
化学
报告基因
生物化学
细胞生物学
酶
生物合成
生物
基因表达
基因
作者
Takuro Matsuoka,Akira Hattori,Shinya Oishi,Mitsugu Araki,Biao Ma,Toshiki Fujii,Norihito Arichi,Yasushi Okuno,Hideaki Kakeya,Sho Yamasaki,Hiroaki Ohno,Shinsuke Inuki
标识
DOI:10.1021/acs.jmedchem.3c01122
摘要
Mucosal-associated invariant T (MAIT) cells are innate-like T cells that are modulated by ligands presented on MHC class I-related proteins (MR1). These cells have attracted attention as potential drug targets because of their involvement in the initial response to infection and various disorders. Herein, we have established the MR1 presentation reporter assay system employing split-luciferase, which enables the efficient exploration of MR1 ligands. Using our screening system, we identified phenylpropanoid derivatives as MR1 ligands, including coniferyl aldehyde, which have an ability to inhibit the MR1-MAIT cell axis. Further, the structure-activity relationship study of coniferyl aldehyde analogs revealed the key structural features of ligands required for MR1 recognition. These results will contribute to identifying a broad range of endogenous and exogenous MR1 ligands and to developing novel MAIT cell modulators.
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