Department of Chemistry , University of Pittsburgh , Pittsburgh , Pennsylvania 15260 , United States.
J Am Chem Soc. 2020 Feb 5;142(5):2193-2197. doi: 10.1021/jacs.9b12718. Epub 2020 Jan 23.
As an emerging approach to protein perturbation, small molecule-induced protein degradation has gained significant attention as both a chemical tool and a potential therapeutic. To enable discrete control over its function, we have developed a broadly applicable approach for the optical activation of small molecule-induced protein degradation. By installing two different photolabile protecting groups, so-called caging groups, onto two different ligands recruiting Von Hippel-Lindau (VHL) and cereblon (CRBN) E3 ubiquitin ligases, our strategy enables light-triggered protein degradation for any small molecule warhead.
作为一种新兴的蛋白质干扰方法,小分子诱导的蛋白质降解作为一种化学工具和潜在的治疗方法引起了广泛关注。为了能够对其功能进行离散控制,我们开发了一种广泛适用于小分子诱导的蛋白质降解的光学激活方法。通过将两个不同的光解保护基团(所谓的“笼状”基团)安装到两个不同的配体上,募集 von Hippel-Lindau (VHL) 和 cereblon (CRBN) E3 泛素连接酶,我们的策略为任何小分子弹头都实现了光触发的蛋白质降解。