Application of Room-Temperature Aprotic and Protic Ionic Liquids for Oxidative Folding of Cysteine-Rich Peptides

作者：Heimer Pascal; Tietze Alesia A; Boehm Miriam; Giernoth Ralf; Kuchenbuch Andrea; Stark Annegret; Leipold Enrico; Heinemann Stefan H; Kandt Christian; Imhof Diana^*

来源：ChemBioChem, 2014, 15(18): 2754-2765.

DOI：10.1002/cbic.201402356

• conotoxins
• cysteine-rich
• ionic liquids
• oxidative folding
• peptide synthesis

The oxidation of the conotoxin mu-SIIIA in different ionic liquids was investigated, and the results were compared with those obtained in [C(2)mim][OAc]. Conversion of the reduced precursor into the oxidized product was observed in the protic ILs methyl-and ethylammonium formate (MAF and EAf, respectively), whereas choline dihydrogenphosphate and Ammoeng 110 failed to yield folded peptide. However, the quality and yield of the peptide obtained in MAF and EAF were lower than in the case of the product from [C(2)mim][OAc]. Reaction conditions (temperature, water content) also had an impact on peptide conversion. A closer look at the activities of mu-SIIIA versions derived from an up-scaled synthesis in [C(2)mim][OAc] revealed a significant loss of the effect on ion channel Na(V)1.4 relative to the buffer-oxidized peptide, whereas digestion of either mu-SIIIA product by trypsin was unaffected. This was attributed to adherence of ions from the IL to the peptide, because the disulfide connectivity is basically the same for the differentially oxidized mu-SIIIA versions.

• 出版日期2014-12-15