Department of Chemical Biology, Max Planck Institute for Molecular Physiology, Otto-Hahn Strasse 11, D-44227 Dortmund, Germany.
J Org Chem. 2013 Mar 15;78(6):2715-9. doi: 10.1021/jo302587g. Epub 2013 Feb 13.
Phosphocholination of eukaryotic host cell proteins has recently been identified as a novel post-translational modification important for bacterial pathogenesis. Here, we describe the first straightforward synthetic strategy for peptides containing phosphocholinated serine, threonine, or tyrosine residues using preformed functional amino acid building blocks, fully compatible with standard Fmoc solid-phase peptide synthesis.
真核宿主细胞蛋白的磷酸胆碱基化最近被鉴定为一种新的翻译后修饰,对于细菌发病机制很重要。在这里,我们描述了使用预形成的功能性氨基酸构建块合成含有磷酸胆碱基化丝氨酸、苏氨酸或酪氨酸残基的肽的第一个直接的合成策略,完全与标准 Fmoc 固相肽合成兼容。