化学
降级(电信)
肽
生物化学
药代动力学
寡肽
细胞生物学
药理学
纤维化
酶
细胞生长
癌症研究
信号转导
生物物理学
动力学
结构-活动关系
受体
肝纤维化
药品
生物相容性材料
磷酸化
作者
Liang Qi,Daimin Luo,Wei Cheng,Qinglin Tang,Jiale Dong,Han Liu,Zhuowen Li,Yanqiu Yuan,Haonan Li,Xianxing Jiang
标识
DOI:10.1021/acs.jmedchem.6c01441
摘要
Abstract Direct depletion of TGF-βR1 may provide more durable suppression of profibrotic signaling than occupancy-driven inhibition, but compact lysosome-directed degraders remain underdeveloped. Here, we report a peptide-based strategy for lysosomal degradation of TGF-βR1 by re-engineering a caveolin-derived antifibrotic scaffold. Structure-guided optimization identified T19 as an improved TGF-βR1-directed sequence, and incorporation of an intrinsic lysosome-targeting module generated P2, which induced time and dose-dependent, lysosome-dependent TGF-βR1 downregulation. Fatty-acid conjugation afforded P2-FA with improved stability and pharmacokinetic properties. P2-FA suppressed profibrotic signaling, reduced α-SMA and COL1A1 expression, and inhibited proliferation and migration of activated LX-2 cells. In a CCl4-induced mouse model, P2-FA attenuated collagen deposition, decreased fibrotic marker expression, and alleviated liver injury. These results identify P2-FA as a pharmacologically improved peptide-based TGF-βR1 degrader and antifibrotic lead.
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