Saito Fumito, Bode Jeffrey W
Laboratorium füer Organische Chemie , Department of Chemistry and Applied Biosciences , ETH Zürich , Zürich , Switzerland 8093 . Email:
Chem Sci. 2017 Apr 1;8(4):2878-2884. doi: 10.1039/c7sc00021a. Epub 2017 Jan 26.
The chemical synthesis of peptide-based [1]rotaxanes (lasso peptides) was achieved by [2]rotaxane formation followed by two chemoselective ligation reactions. Our approach enabled incorporation of various peptide sequences into a common rotaxane structure. The synthetic lasso peptides were characterized by NMR, chromatography, and partial degradation by proteases. A linear peptide epitope grafted onto the rotaxane scaffold showed significantly improved proteolytic stability.
基于肽的[1]轮烷(套索肽)的化学合成是通过[2]轮烷形成,然后进行两个化学选择性连接反应实现的。我们的方法能够将各种肽序列整合到一个共同的轮烷结构中。合成的套索肽通过核磁共振、色谱法以及蛋白酶的部分降解进行表征。接枝到轮烷支架上的线性肽表位显示出显著提高的蛋白水解稳定性。