Department of Biochemistry & Biophysics, Texas A&M University, College Station, Texas 77843, United States.
X-Chem Inc., 100 Beaver Street, Waltham, Massachusetts 02453, United States.
ACS Infect Dis. 2024 May 10;10(5):1561-1575. doi: 10.1021/acsinfecdis.3c00592. Epub 2024 Apr 5.
DNA-encoded chemical library (DEL) technology provides a time- and cost-efficient method to simultaneously screen billions of compounds for their affinity to a protein target of interest. Here we report its use to identify a novel chemical series of inhibitors of the thioesterase activity of polyketide synthase 13 (Pks13) from (Mtb). We present three chemically distinct series of inhibitors along with their enzymatic and Mtb whole cell potency, the measure of on-target activity in cells, and the crystal structures of inhibitor-enzyme complexes illuminating their interactions with the active site of the enzyme. One of these inhibitors showed a favorable pharmacokinetic profile and demonstrated efficacy in an acute mouse model of tuberculosis (TB) infection. These findings and assay developments will aid in the advancement of TB drug discovery.
DNA 编码化学文库 (DEL) 技术提供了一种高效、省时的方法,可以同时筛选数十亿种化合物,以确定它们与目标蛋白的亲和力。在这里,我们报告了使用该技术从 (Mtb)中鉴定新型聚酮合酶 13 (Pks13) 硫酯酶活性抑制剂的化学系列。我们展示了三种具有不同化学结构的抑制剂及其酶活性和 Mtb 全细胞活力,这是细胞中靶标活性的衡量标准,以及抑制剂-酶复合物的晶体结构,阐明了它们与酶活性位点的相互作用。其中一种抑制剂表现出良好的药代动力学特性,并在急性结核分枝杆菌 (TB) 感染小鼠模型中显示出疗效。这些发现和检测方法的发展将有助于推进结核病药物的发现。