Jurkat细胞
生物信息学
CTL公司*
肽
对接(动物)
抗体
体外
细胞生物学
蛋白质-蛋白质相互作用
拟肽
化学
合理设计
细胞毒性T细胞
计算生物学
癌症研究
生物
T细胞
生物化学
免疫系统
免疫学
医学
护理部
基因
遗传学
作者
Rebecca J. Boohaker,Vijaya Sambandam,Isaac Segura,James Miller,Mark J. Suto,Bo Xu
标识
DOI:10.1016/j.canlet.2018.04.031
摘要
We report here the rational design and validation of a peptide inhibitor to the PD-1/PD-L1 interaction as an attempt to develop a viable alternative to current inhibitory antibodies. We demonstrated, by biolayer interferometry and in silico docking simulations, that a PD-L1 peptide mimetic (PL120131) can interfere with the PD-1/PD-L1 interaction by binding to PD-1. We show that PL120131 is capable of inhibiting PD-1 mediated apoptotic signaling pathway and rescuing Jurkat cells and primary lymphocytes from apoptosis. Additionally, we show that PL120131 treatment allows for CTL anti-tumor activity. Furthermore, PL120131 can maintain co-culture survivability and activity of T Cells in a 3D co-culture model better than the anti-PD-1 blocking antibody. Together, the characterization of this PD-1/PD-L1 inhibiting peptide provides insight regarding the ability to inhibit PD-L1 binding while maintaining CTL viability and activity that can further the development of alternatives to antibody based immunotherapies.
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