Neumann Heinz, Peak-Chew Sew Y, Chin Jason W
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 0QH England, UK.
Nat Chem Biol. 2008 Apr;4(4):232-4. doi: 10.1038/nchembio.73. Epub 2008 Feb 17.
N(epsilon)-acetylation of lysine (1) is a reversible post-translational modification with a regulatory role that rivals that of phosphorylation in eukaryotes. No general methods exist to synthesize proteins containing N(epsilon)-acetyllysine (2) at defined sites. Here we demonstrate the site-specific incorporation of N(epsilon)-acetyllysine in recombinant proteins produced in Escherichia coli via the evolution of an orthogonal N(epsilon)-acetyllysyl-tRNA synthetase/tRNA(CUA) pair. This strategy should find wide applications in defining the cellular role of this modification.
赖氨酸的N(ε)-乙酰化(1)是一种可逆的翻译后修饰,其调控作用在真核生物中可与磷酸化相媲美。目前还没有在特定位点合成含有N(ε)-乙酰赖氨酸(2)的蛋白质的通用方法。在此,我们通过进化出一对正交的N(ε)-乙酰赖氨酰-tRNA合成酶/tRNA(CUA),证明了N(ε)-乙酰赖氨酸在大肠杆菌中产生的重组蛋白中的位点特异性掺入。该策略在确定这种修饰的细胞作用方面应会有广泛的应用。