School of Chinese Materia Medica, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing 210023, China.
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai 201203, China.
J Med Chem. 2024 Jan 25;67(2):1079-1092. doi: 10.1021/acs.jmedchem.3c01463. Epub 2024 Jan 3.
The DNA-encoded library (DEL) is a powerful hit generation tool for chemical biology and drug discovery; however, the optimization of DEL hits remained a daunting challenge for the medicinal chemistry community. In this study, hit compounds targeting the WIN binding domain of WDR5 were discovered by the initial three-cycle linear DEL selection, and their potency was further enhanced by a cascade DEL selection from the focused DEL designed based on the original first run DEL hits. As expected, these new compounds from the second run of focused DEL were more potent WDR5 inhibitors in the protein binding assay confirmed by the off-DNA synthesis. Interestingly, selected inhibitors exhibited good antiproliferative activity in two human acute leukemia cell lines. Taken together, this new cascade DEL selection strategy may have tremendous potential for finding high-affinity leads against WDR5 and provide opportunities to explore and optimize inhibitors for other targets.
DNA 编码文库 (DEL) 是化学生物学和药物发现的强大命中生成工具;然而,DEL 命中的优化仍然是药物化学界面临的艰巨挑战。在这项研究中,通过初始的三轮线性 DEL 选择发现了针对 WDR5 的 WIN 结合域的命中化合物,并且通过基于原始第一轮 DEL 命中设计的聚焦 DEL 进行级联 DEL 选择进一步提高了它们的效力。正如预期的那样,这些来自第二轮聚焦 DEL 的新化合物在蛋白质结合测定中是更有效的 WDR5 抑制剂,这一点通过非 DNA 合成得到了证实。有趣的是,所选抑制剂在两种人急性白血病细胞系中表现出良好的增殖抑制活性。总之,这种新的级联 DEL 选择策略可能具有发现针对 WDR5 的高亲和力先导化合物的巨大潜力,并为探索和优化其他靶标抑制剂提供机会。