Sakamoto Ken, Tsuda Shugo, Mochizuki Masayoshi, Nohara Yukie, Nishio Hideki, Yoshiya Taku
Peptide Institute, Inc., 7-2-9 Saito-Asagi, Ibaraki-shi, Osaka, 567-0085, Japan.
Chemistry. 2016 Dec 12;22(50):17940-17944. doi: 10.1002/chem.201604320. Epub 2016 Nov 3.
Various bioactive proteins have been synthesized by native chemical ligation (NCL) and its combination with subsequent desulfurization (e.g., conversion from Cys to Ala). In NCL, excess 4-mercaptophenylacetic acid (MPAA) is generally added to facilitate the reaction. However, co-elution of MPAA with the ligation product during preparative high-performance liquid chromatography sometimes reduces its usefulness. In addition, contamination of MPAA disturbs subsequent desulfurization. Here, we report for the first time that imidazole can be adopted as an alternative to MPAA in NCL using a peptide-alkylthioester. The efficiency of the imidazole-aided NCL (Im-NCL) is similar to that of traditional MPAA-aided NCL. As model cases, we successfully synthesized adiponectin(19-107) and [Ser(PO H ) ]-ubiquitin using Im-NCL with a one-pot desulfurization.
通过天然化学连接(NCL)及其与后续脱硫反应(例如,从半胱氨酸转化为丙氨酸)的结合,已经合成了各种生物活性蛋白质。在NCL中,通常会添加过量的4-巯基苯乙酸(MPAA)以促进反应。然而,在制备型高效液相色谱过程中,MPAA与连接产物的共洗脱有时会降低其效用。此外,MPAA的污染会干扰后续的脱硫反应。在此,我们首次报道在使用肽-烷基硫酯的NCL中,咪唑可以用作MPAA的替代品。咪唑辅助的NCL(Im-NCL)的效率与传统的MPAA辅助的NCL相似。作为实例,我们使用Im-NCL和一锅法脱硫成功合成了脂联素(19-107)和[Ser(POH)]-泛素。