Department of Chemical Biology, Max-Planck Institute of Molecular Physiology, Otto-Hahn Strasse 11, D-44227, Dortmund, Germany.
Org Lett. 2011 Nov 18;13(22):6014-7. doi: 10.1021/ol2024696. Epub 2011 Oct 26.
The first straightforward building block based (non-interassembly) synthesis of peptides containing adenylylated serine and threonine residues is described. Key features include final global acidolytic protective group removal as well as full compatibility with standard Fmoc solid-phase peptide synthesis (SPPS). The described Thr-AMP SPPS-building block has been employed in the synthesis of the Thr-adenylylated sequence of human GTPase CDC42 (Ac-SEYVP-T(AMP)-VFDNYGC-NH(2)). Further, we demonstrate proof-of-concept for the synthesis of an Ser-adenylylated peptide (Ac-GSGA-S(AMP)-AGSGC-NH(2)) from the corresponding adenylylated serine building block.
首次描述了基于第一个直链砌块(非组装)的合成含有腺苷酰化丝氨酸和苏氨酸残基的肽。关键特点包括最终的全局酸性裂解保护基团去除以及与标准 Fmoc 固相肽合成(SPPS)完全兼容。所描述的 Thr-AMP SPPS 砌块已用于人 GTPase CDC42(Ac-SEYVP-T(AMP)-VFDNYGC-NH(2))的 Thr-腺苷酰化序列的合成。此外,我们还从相应的腺苷酰化丝氨酸砌块合成了一个 Ser-腺苷酰化肽(Ac-GSGA-S(AMP)-AGSGC-NH(2)),证明了这一概念的可行性。