School of Pharmacy, Second Military Medical University (Navy Medical University), Shanghai 200433, China.
Institute of Translational Medicine, Shanghai University, Shanghai 200444, China.
J Med Chem. 2022 Dec 8;65(23):15725-15737. doi: 10.1021/acs.jmedchem.2c01243. Epub 2022 Nov 28.
Proteolysis-targeting chimera (PROTAC) is emerging as a promising technology in targeted protein degradation and drug discovery. However, there is still a lack of effective chemical tools to real-time detect and track the protein degradation. Herein, the first fluorescent and theranostic PROTACs were designed for imaging the degradation of nicotinamide phosphoribosyltransferase (NAMPT) in living cells. Compound was proven to be an environmentally sensitive fluorescent PROTAC, which efficiently degraded NAMPT (DC = 8.4 nM) and enabled the visualization of degradation in A2780 cells. As a theranostic agent, PROTAC led to significant reduction of nicotinamide adenine dinucleotide (NAD) and exerted potent antitumor activities both in vitro and in vivo. Collectively, this proof-of-concept study provides a new strategy for the real-time visualization of the process of protein degradation and the improvement of diagnosis and therapeutic efficacy of PROTACs.
蛋白水解靶向嵌合体(PROTAC)作为一种新兴的靶向蛋白降解和药物发现技术,正在引起广泛关注。然而,目前仍缺乏有效的化学工具来实时检测和跟踪蛋白降解。在此,我们设计了第一个荧光和治疗性 PROTAC,用于在活细胞中成像烟酰胺磷酸核糖转移酶(NAMPT)的降解。实验证明,化合物 是一种环境敏感的荧光 PROTAC,能够有效降解 NAMPT(DC = 8.4 nM),并实现 A2780 细胞中降解的可视化。作为一种治疗性试剂,PROTAC 导致烟酰胺腺嘌呤二核苷酸(NAD)的显著减少,并在体外和体内均表现出强大的抗肿瘤活性。总之,这项概念验证研究为实时可视化蛋白降解过程以及提高 PROTAC 的诊断和治疗效果提供了一种新策略。