Department of Chemistry and Biochemistry, University of California, La Jolla, California 92093, United States.
J Med Chem. 2023 Feb 23;66(4):2789-2803. doi: 10.1021/acs.jmedchem.2c01843. Epub 2023 Feb 3.
Human carbonic anhydrase II (hCAII) is a metalloenzyme essential to critical physiological processes in the body. hCA inhibitors are used clinically for the treatment of indications ranging from glaucoma to epilepsy. Targeted protein degraders have emerged as a promising means of inducing the degradation of disease-implicated proteins by using the endogenous quality control mechanisms of a cell. Here, a series of heterobifunctional degrader candidates targeting hCAII were developed from a simple aryl sulfonamide fragment. Degrader candidates were functionalized to produce either cereblon E3 ubiquitin ligase (CRBN) recruiting proteolysis targeting chimeras (PROTACs) or adamantyl-based hydrophobic tags (HyTs). Screens in HEK293 cells identified two PROTAC small-molecule degraders of hCA. Optimization of linker length and composition yielded a degrader with sub-nanomolar potency and sustained depletion of hCAII over prolonged treatments. Mechanistic studies suggest that this optimized degrader depletes hCAII through the same mechanism as previously reported CRBN-recruiting heterobifunctional degraders.
人碳酸酐酶 II(hCAII)是一种金属酶,对体内关键生理过程至关重要。hCA 抑制剂临床上用于治疗从青光眼到癫痫等多种适应症。靶向蛋白降解剂已成为一种很有前途的方法,可以利用细胞的内源性质量控制机制诱导疾病相关蛋白的降解。在这里,从简单的芳基磺酰胺片段开发了一系列靶向 hCAII 的杂双功能降解剂候选物。降解剂候选物被功能化以产生 either cereblon E3 泛素连接酶(CRBN)招募蛋白水解靶向嵌合体(PROTAC)或金刚烷基疏水标签(HyT)。在 HEK293 细胞中的筛选鉴定出两种 hCA 的 PROTAC 小分子降解剂。对连接体长度和组成的优化得到了一种具有亚纳摩尔效力的降解剂,并在延长治疗过程中持续耗尽 hCAII。机制研究表明,这种优化的降解剂通过与先前报道的 CRBN 招募杂双功能降解剂相同的机制耗尽 hCAII。