Sorbara Marie, Cristol Margot, Cornebois Anaïs, Desrumeaux Klervi, Cordelier Pierre, Bery Nicolas
Université de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, 31100 Toulouse, France.
Université de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, 31100 Toulouse, France; Sanofi, Large Molecule Research, 94400 Vitry-sur-Seine, France.
STAR Protoc. 2024 Dec 20;5(4):103413. doi: 10.1016/j.xpro.2024.103413. Epub 2024 Oct 24.
Here, we provide a protocol for the identification of E3 ubiquitin ligases that are functional when implemented as biodegraders using a cell-based screening assay. We describe steps for establishing a stable cell line expressing a GFP-tagged protein of interest (POI), preparing a sub-library of E3 ligases to screen, and performing the cell-based screening. This protocol can be broadly applied to identify any functional E3 ligase in a biodegrader setting. For complete details on the use and execution of this protocol, please refer to Cornebois et al..
在此,我们提供了一种用于鉴定E3泛素连接酶的方案,这些连接酶在作为生物降解剂实施时,通过基于细胞的筛选试验发挥功能。我们描述了建立表达感兴趣的绿色荧光蛋白(GFP)标记蛋白(POI)的稳定细胞系、制备用于筛选的E3连接酶亚文库以及进行基于细胞的筛选的步骤。该方案可广泛应用于在生物降解剂环境中鉴定任何功能性E3连接酶。有关该方案使用和执行的完整详细信息,请参考科尔内布瓦等人的研究。