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Imidazole-Aided Native Chemical Ligation: Imidazole as a One-Pot Desulfurization-Amenable Non-Thiol-Type Alternative to 4-Mercaptophenylacetic Acid.

Ken SakamotoShugo TsudaMasayoshi MochizukiYukie NoharaHideki NishioTaku Yoshiya
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2016)
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(PO3 H2 )65 ]-ubiquitin using Im-NCL with a one-pot desulfurization.
Keyphrases
  • high performance liquid chromatography
  • metabolic syndrome
  • mass spectrometry
  • tandem mass spectrometry
  • simultaneous determination
  • type diabetes
  • small molecule
  • insulin resistance
  • drinking water
  • human health