TLR2型
体内
受体
信号转导
体外
化学
药理学
细胞生物学
生物
生物化学
先天免疫系统
遗传学
作者
Pragnesh Mistry,Michelle Laird,Ryan S. Schwarz,Shannon N. Greene,Tristan Dyson,Greg A. Snyder,Tsan Sam Xiao,Jay Chauhan,Steven Fletcher,Vladimir Y. Toshchakov,Alexander D. MacKerell,Stefanie N. Vogel
标识
DOI:10.1073/pnas.1422576112
摘要
Significance Excess Toll-like receptor 2 (TLR2) signaling has been implicated in numerous inflammatory diseases, yet there is no TLR2 inhibitor licensed for human use. Using computer-aided drug design (CADD), we identified a compound, C 16 H 15 NO 4 (C29), and a derivative, ortho -vanillin, that inhibit TLR2 signaling in vitro and in vivo. Our findings also revealed unexpected differences between TLR2/1 and TLR2/6 signaling in mice vs. humans. Importantly, our data provide proof of principle that the CADD-targeted BB loop pocket residues are critical for TLR2 signaling and may be targeted therapeutically.
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