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. 2014 Jun 18;50(61):8316–8319. doi: 10.1039/c4cc03065f

Fig. 1. Synthesis of a difficult peptide sequence from influenza virus Hemagglutinin.11 Analytical HPLC traces of crude product prepared using: (A) conventional automated SPPS, (a = target peptide, b = deletion of Met1-Glu2-Asp3, c = deletion of Met1-Glu2, d = deletion of Glu1, e = t-butylated product). (B) Conventional automated SPPS with backbone protection at Ala9. (C) Automated microwave assisted SPPS. (D) Automated microwave-assisted SPPS backbone protection at Ala9. (E) MALDI-MS of target peptide, a, (calculated mass [M + H]+ = 1481.6 m/z) peptide cleavage conditions: TFA/TMSBr/thioanisole/ethanedithiol (1.0 : 0.05 : 0.05 : 0.025 v/v), 1.0 h. HPLC conditions: RP-C18, 0–50% (0.1% TFA, 90% CH3CN) in 30 min, 1 mL min–1.

Fig. 1