Lau S-Y, Siau J W, Sobota R M, Wang C-I, Zhong P, Lane D P, Ghadessy F J
p53 Laboratory (p53Lab), Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, Singapore, Singapore.
Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), 61 Biopolis Dr, Singapore, Singapore.
Protein Eng Des Sel. 2018 Jul 1;31(7-8):301-312. doi: 10.1093/protein/gzy018.
Engineered non-antibody scaffold proteins constitute a rapidly growing technology for diagnostics and modulation/perturbation of protein function. Here, we describe the rapid and systematic development of high-affinity 10FN3 domain inhibitors of the MDM2 and MDMX proteins. These are often overexpressed in cancer and represent attractive drug targets. Using facile in vitro expression and pull-down assay methodology, numerous design iterations addressing insertion site(s) and spacer length were screened for optimal presentation of an MDM2/X dual peptide inhibitor in the 10FN3 scaffold. Lead inhibitors demonstrated robust, on-target cellular inhibition of MDM2/X leading to activation of the p53 tumor suppressor. Significant improvement to target engagement was observed by increasing valency within a single 10FN3 domain, which has not been demonstrated previously. We further established stable reporter cell lines with tunable expression of EGFP-fused 10FN3 domain inhibitors, and showed their intracellular location to be contingent on target engagement. Importantly, competitive inhibition of MDM2/X by small molecules and cell-penetrating peptides led to a readily observable phenotype, indicating significant potential of the developed platform as a robust tool for cell-based drug screening.
工程化非抗体支架蛋白是一种用于蛋白质功能诊断及调节/干扰的快速发展的技术。在此,我们描述了MDM2和MDMX蛋白的高亲和力10FN3结构域抑制剂的快速系统开发。这些蛋白在癌症中常过度表达,是有吸引力的药物靶点。利用简便的体外表达和下拉分析方法,针对插入位点和间隔长度进行了多次设计迭代,以筛选出10FN3支架中MDM2/X双肽抑制剂的最佳呈现方式。先导抑制剂对MDM2/X表现出强大的、靶向性的细胞抑制作用,从而激活p53肿瘤抑制因子。通过增加单个10FN3结构域内的价态,观察到靶点结合有显著改善,这在之前尚未得到证实。我们进一步建立了稳定的报告细胞系,其可调控表达EGFP融合的10FN3结构域抑制剂,并表明其细胞内定位取决于靶点结合。重要的是,小分子和细胞穿透肽对MDM2/X的竞争性抑制导致了易于观察的表型,表明所开发的平台作为基于细胞的药物筛选的强大工具具有巨大潜力。