Yoshiya Taku, Ito Nui, Kimura Tooru, Kiso Yoshiaki
Department of Medicinal Chemistry, Division of Medicinal Chemical Sciences, Center for Frontier Research in Medicinal Science, 21st Century COE Program, Kyoto Pharmaceutical University, Yamashina-ku, Kyoto, Japan.
J Pept Sci. 2008 Nov;14(11):1203-8. doi: 10.1002/psc.1053.
A novel strategy for a more efficient synthesis of difficult sequence-containing peptides, the S-acyl isopeptide method, was developed and successfully applied. A model pentapeptide Ac-Val-Val-Cys-Val-Val-NH2 was synthesized via its water-soluble S-acyl isopeptide using an S-acyl isodipeptide unit, Boc-Cys(Fmoc-Val)-OH. An S-acyl isopeptide possessing excellent water solubility could be readily and quantitatively converted to the native peptide via an S--N intramolecular acyl migration reaction at pH 7.4. Thus, the S-acyl isopeptide method provides a useful tool in peptide chemistry.
一种用于更高效合成含难序列肽段的新策略——S-酰基异肽法被开发并成功应用。通过使用S-酰基异二肽单元Boc-Cys(Fmoc-Val)-OH,经由其水溶性S-酰基异肽合成了模型五肽Ac-Val-Val-Cys-Val-Val-NH2。具有优异水溶性的S-酰基异肽可在pH 7.4条件下通过S→N分子内酰基迁移反应轻松且定量地转化为天然肽段。因此,S-酰基异肽法为肽化学提供了一种有用的工具。