Sakamoto Ken, Tsuda Shugo, Nishio Hideki, Yoshiya Taku
Peptide Institute, Inc., Ibaraki-shi, Osaka 567-0085, Japan.
Chem Commun (Camb). 2017 Nov 9;53(90):12236-12239. doi: 10.1039/c7cc07817j.
1,2,4-Triazole facilitated native chemical ligation (NCL) between peptide-MeNbz (MeNbz: N-acyl-N'-methyl-benzimidazolinone) and a cysteinyl peptide in the absence of thiol additives. The method enabled one-pot desulfurization and iodine oxidation after NCL. Additionally, the direct isolation of the target peptide from the NCL reaction mixture with an activated thiopropyl-Sepharose resin was achieved.
1,2,4-三唑在无硫醇添加剂的情况下促进了肽-MeNbz(MeNbz:N-酰基-N'-甲基苯并咪唑啉酮)与半胱氨酰肽之间的天然化学连接(NCL)。该方法能够在NCL后进行一锅法脱硫和碘氧化。此外,还实现了用活化的硫丙基-琼脂糖树脂从NCL反应混合物中直接分离目标肽。