化学
小分子
白细胞介素2
白细胞介素2受体
受体
细胞因子
DNA
药物发现
立体化学
计算生物学
生物化学
免疫学
体外
生物
细胞毒性T细胞
作者
Adrián Gironda-Martínez,Émile M. D. Gorre,Luca Prati,Jean-François Gosalbes,Sheila Dakhel,Samuele Cazzamalli,Florent Samain,Etienne J. Donckèle,Dario Neri
标识
DOI:10.1021/acs.jmedchem.1c01693
摘要
Interleukin-2 (IL2) is a pro-inflammatory cytokine that plays a crucial role in immunity, which is increasingly being used for therapeutic applications. There is growing interest in developing IL2-based therapeutics which do not interact with the alpha subunit of the IL2 receptor (CD25) as this protein is primarily found on immunosuppressive regulatory T cells (Tregs). Screenings of a new DNA-encoded library, comprising 669,240 members, provided a novel series of IL2 ligands, subsequently optimized by medicinal chemistry. One of these molecules (compound 18) bound to IL2 with a dissociation constant of 0.34 μM was able to form a kinetically stable complex with IL2 in size-exclusion chromatography and recognized the CD25-binding site as evidenced by competition experiments with the NARA1 antibody. Compound 18 and other members of the series may represent the starting point for the discovery of potent small-molecule modulators of IL2 activity, abrogating the binding to CD25.
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