化学
蛋白质水解
靶蛋白
小分子
共价键
蛋白质降解
生物化学
药物发现
蛋白质-蛋白质相互作用
嵌合体(遗传学)
配体(生物化学)
组合化学
计算生物学
酶
生物
受体
基因
有机化学
作者
Hyeonjun Lee,Ju Yeon Lee,Hyunsoo Jang,Hyunsoo Jang,Hye Young Cho,Minhee Kang,Sang Hyun Bae,Eunji Kim,Suin Kim,Eunji Kim,Eunji Kim,Jaebong Jang,Jin Young Kim,Young Ho Jeon
标识
DOI:10.1016/j.ejmech.2023.115929
摘要
Targeted protein degradation (TPD) technology, such as proteolysis-targeting chimera (PROTAC), has become a new therapeutic modality. However, the degradation of undruggable proteins, such as those involved in protein-protein interactions (PPIs), using PROTAC is still limited owing to the difficulties in finding small-molecule binders of these proteins. To identify new chemical moieties that bind to the target sites of the protein of interest (POI), we conducted a site-specific and fragment-based covalent ligand screening using liquid chromatography-tandem mass spectrometry (LC-MS/MS). To apply the selected hits to the PROTAC approach, two-dimensional (2D) nuclear magnetic resonance (NMR) experiments were performed to evaluate the reversible binding of their analogs without covalent warheads. To proof the proposed approach, human mouse double minute (MDM)2 was selected as a model system since it is involved in PPIs and is known to be a degradable target protein. Western blot analysis showed that newly synthesized PROTACs, incorporated reversible analogs of screening hits, affected degradation in a dose- and time-dependent manner. This methodology makes it possible to use PROTAC technology to exploit previously undruggable proteins for TPD.
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