肽库
肽
噬菌体展示
免疫系统
分子生物学
抗体
化学
癌症研究
生物
肽序列
生物化学
免疫学
基因
作者
Jinping Tao,Fei Wang,Ziqing Zeng,Wenyuan Zhou,Zilei Wang,Chengxue He,Jinyu Zhu,Chuanke Zhao,Hua Zhu
标识
DOI:10.1021/acs.molpharmaceut.4c00884
摘要
T-cell immunoglobulin and mucin domain-3 (TIM3) is an immune checkpoint that plays a negative regulatory role in the immune response. TIM3-targeted drugs inhibit this negative regulation, thereby modulating the level of immune response activation. In the previous investigation, several peptides targeting TIM3 were identified through screening from a phage peptide library. In this research, three peptides were selected to construct the radioactive molecular probes according to the characteristic that targeting TIM3 drugs would lead to the increase of interferon-γ (IFN-γ) secretion. Molecular docking was performed to assess the binding properties of the selected peptides with the TIM3 protein. To further enhance the targeting properties, one of the peptides with a higher-affinity peptide was structurally modified. Then,
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