炎症体
上睑下垂
化学
细胞内
先天免疫系统
细胞生物学
NLRP1
程序性细胞死亡
生物化学
受体
半胱氨酸蛋白酶
生物
细胞凋亡
作者
Qifeng Chen,Alvin Wang,Dominic J. Covelli,Abir Bhattacharjee,Qinghui Wang,Elizabeth L. Orth-He,Sahana D. Rao,Hsin‐Che Huang,Daniel P. Ball,Jeffrey C. Hsiao,Daniel A. Bachovchin
标识
DOI:10.1021/acs.jmedchem.2c01535
摘要
Inflammasomes are innate immune signaling platforms that trigger pyroptotic cell death. NLRP1 and CARD8 are related human inflammasomes that detect similar danger signals, but NLRP1 has a higher activation threshold and triggers a more inflammatory form of pyroptosis. Both sense the accumulation of intracellular peptides with Xaa-Pro N-termini, but Xaa-Pro peptides on their own without a second danger signal only activate the CARD8 inflammasome. We recently reported that a dual inhibitor of the Xaa-Pro-cleaving M24B aminopeptidases PEPD and XPNPEP1 called CQ31 selectively activates the CARD8 inflammasome by inducing the build-up of Xaa-Pro peptides. Here, we performed structure–activity relationship studies on CQ31 to develop the optimized dual PEPD/XPNPEP1 inhibitor CQ80 that more effectively induces CARD8 inflammasome activation. We anticipate that CQ80 will become a valuable tool to study the basic biology and therapeutic potential of selective CARD8 inflammasome activation.
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