Department of Biochemistry, Chemistry and Pharmacy, Institute for Pharmaceutical Chemistry, Goethe University, Frankfurt, Germany.
Structural Genomics Consortium, Buchmann Institute for Molecular Life Sciences, Goethe University, Frankfurt, Germany.
J Cell Biochem. 2024 Nov;125(11):e30380. doi: 10.1002/jcb.30380. Epub 2023 Feb 13.
Induction of Atg8-family protein (LC3/GABARAP proteins in human) interactions with target proteins of interest by proximity-inducing small molecules offers the possibility for novel targeted protein degradation approaches. However, despite intensive screening campaigns during the last 5 years, no potent ligands for LC3/GABARAPs have been developed, rendering this approach largely unexplored and unsuitable for therapeutic exploitation. In this Viewpoint, we analyze the reported attempts identifying LC3/GABARAP inhibitors and provide our own point of view why no potent inhibitors have been found. Additionally, we designate reasonable directions for the identification of potent and probably selective LC3/GABARAP inhibitors for alternative therapeutic applications.
诱导 Atg8 家族蛋白(LC3/GABARAP 蛋白在人类中)与目标蛋白的相互作用通过邻近诱导小分子提供了新的靶向蛋白降解方法的可能性。然而,尽管在过去 5 年中进行了密集的筛选活动,但尚未开发出有效的 LC3/GABARAP 配体,使得这种方法在很大程度上未被探索,不适合治疗性利用。在本观点中,我们分析了报告的鉴定 LC3/GABARAP 抑制剂的尝试,并提出了我们自己的观点,即为什么没有发现有效的抑制剂。此外,我们指定了鉴定有效且可能具有选择性的 LC3/GABARAP 抑制剂的合理方向,以用于替代治疗应用。