Imidazole‐Aided Native Chemical Ligation: Imidazole as a One‐Pot Desulfurization‐Amenable Non‐Thiol‐Type Alternative to 4‐Mercaptophenylacetic Acid |
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Authors: | Ken Sakamoto Dr. Shugo Tsuda Dr. Masayoshi Mochizuki Yukie Nohara Dr. Hideki Nishio Dr. Taku Yoshiya |
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Affiliation: | 1. https://www.peptide.co.jp/en;2. Peptide Institute, Inc., Osaka, Japan |
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Abstract: | 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(PO3H2)65]‐ubiquitin using Im‐NCL with a one‐pot desulfurization. |
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Keywords: | chemical protein synthesis desulfurization imidazole native chemical ligation thiol additive free |
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