Eger Silvia, Scheffner Martin, Marx Andreas, Rubini Marina
Department of Chemistry, Konstanz Research School Chemical Biology, University of Konstanz, Konstanz, Germany.
Methods Mol Biol. 2012;832:589-96. doi: 10.1007/978-1-61779-474-2_41.
The conjugation of poly-ubiquitin chains is a widespread post-translational modification of proteins that plays a role in many different cellular processes. Notably, the biological function of the attached ubiquitin chain depends on which lysine residue is used for chain formation. Here, we report a method for the modular synthesis of site-specifically linked ubiquitin dimers, which is based on click reaction between two artificial amino acids. In this way, it is possible to synthesize all seven naturally occurring ubiquitin connectivities, thus giving access to all ubiquitin dimers. Furthermore, this method can be generally applied to link ubiquitin to any substrate protein or even to link any two proteins site specifically.
多聚泛素链的缀合是一种广泛存在的蛋白质翻译后修饰,在许多不同的细胞过程中发挥作用。值得注意的是,附着的泛素链的生物学功能取决于用于链形成的赖氨酸残基。在这里,我们报告了一种基于两个人工氨基酸之间的点击反应的位点特异性连接泛素二聚体的模块化合成方法。通过这种方式,可以合成所有七种天然存在的泛素连接方式,从而获得所有泛素二聚体。此外,该方法通常可用于将泛素连接到任何底物蛋白上,甚至可以位点特异性地连接任何两种蛋白质。