Pharmaxis Ltd., 20 Rodborough Road, Frenchs Forest, NSW 2086, Australia.
School of Chemistry, The University of Sydney, Sydney, New South Wales 2006, Australia.
J Med Chem. 2023 Aug 24;66(16):11216-11236. doi: 10.1021/acs.jmedchem.3c00665. Epub 2023 Aug 3.
Mixed Lineage Kinase domain-Like pseudokinase (MLKL) is implicated in a broad range of diseases due to its role as the ultimate effector of necroptosis and has therefore emerged as an attractive drug target. Here, we describe the development of PROteolysis TArgeting Chimeras (PROTACs) as a novel approach to knock down MLKL through chemical means. A series of candidate degraders were synthesized from a high-affinity pyrazole carboxamide-based MLKL ligand leading to the identification of a PROTAC molecule that effectively degraded MLKL and completely abrogated cell death in a TSZ model of necroptosis. By leveraging the innate ability of these PROTACs to degrade MLKL in a dose-dependent manner, the quantitative relationship between MLKL levels and necroptosis was interrogated. This work demonstrates the feasibility of targeting MLKL using a PROTAC approach and provides a powerful tool to further our understanding of the role of MLKL within the necroptotic pathway.
混合谱系激酶结构域样伪激酶(MLKL)作为细胞坏死的最终效应因子,在多种疾病中发挥作用,因此成为一个有吸引力的药物靶点。在这里,我们描述了使用 PROteolysis TArgeting Chimeras(PROTAC)作为一种通过化学手段敲低 MLKL 的新方法。从高亲和力吡唑甲酰胺基 MLKL 配体合成了一系列候选降解剂,从而鉴定出一种 PROTAC 分子,该分子可有效降解 MLKL,并完全阻断 TSZ 细胞坏死模型中的细胞死亡。通过利用这些 PROTAC 以剂量依赖的方式内在降解 MLKL 的能力,研究了 MLKL 水平与细胞坏死之间的定量关系。这项工作证明了使用 PROTAC 方法靶向 MLKL 的可行性,并提供了一个强大的工具来进一步了解 MLKL 在细胞坏死途径中的作用。