化学
提吉特
内化
双功能
小分子
免疫疗法
癌症研究
联轴节(管道)
抗体
生物化学
抑制器
靶向治疗
单克隆抗体
免疫系统
细胞生物学
分子识别
结构-活动关系
肽
生物物理学
生物活性
组合化学
细胞毒性
作者
Francesco Merlino,Valentina Pagliara,Vincenzo Maria D’Amore,Giovanna Polcaro,Francesco Saverio Di Leva,Pasquale Russomanno,Diego Brancaccio,Greta Donati,Isidora Diakogiannaki,Ida Boccino,Luigi Liguori,Jussara Amato,Simona Marzano,Anella Saviano,Vincenzo Mazzarella,Jacek Plewka,Pierfausto Seneci,Daniela Arosio,F Maione,Łukasz Skalniak
标识
DOI:10.1021/acs.jmedchem.5c02586
摘要
Antibodies targeting PD-1 and PD-L1 have achieved considerable success against various cancers, however their effectiveness is limited as both therapeutic and diagnostic tools. Meanwhile, small organic molecules and macrocyclic peptides are currently at various stages of development as modulators of the PD-1/PD-L1 axis. Here, we report an array of low molecular weight anti-PD-L1 macrocyclic peptides, among which two─ FM2 and FM213 ─emerged as promising bifunctional suppressors of PD-1/PD-L1 binding. Through a compound-centric proteomic approach, we demonstrated that FM213 robustly binds to PD-L1 in NSCLC cells and exosomes. Furthermore, at its highest non-cytotoxic concentration (2 μM), FM213 (i) significantly enhances recognition and destruction of NSCLC cells by human PBMCs, and (ii) promotes the internalization of cell-surface PD-L1 into the cytosol, leading to its degradation via a lysosome-dependent pathway. Finally, coinhibition of TIGIT and PD-L1 by D TBP-3, a TIGIT inhibitor, and FM213, respectively, enhances the antitumor immunity of anti-PD-L1 ligands.
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