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Title: Synthesis of peptide fragments of the hemagglutinin of influenza virus A/Aichi/2/68 (H/sub 3/N/sub 2/)

Journal Article · · Sov. J. Bioorg. Chem. (Engl. Transl.); (United States)
OSTI ID:5244049

Peptides corresponding to sections 122-133, 136-147, and 154-164 of the heavy chain of the hemagglutinin of influenza virus A/Aichi/2/68 (H/sub 3/N/sub 2/) have been synthesized. The synthesis was performed by the stepwise growth of the peptide chain by means of activated esters of Boc-amino acids and the condensation of peptide blocks by the carbodiimide method in solution. The colored 2-(4-(phenylazo)benylsulfonyl)ethyl group, which can be removed by bases, was used for the protection of the C-terminal carboxy groups of the peptides and peptide blocks, facilitating the purification of the peptides synthesized. After the elimination of the N- and C-terminal carboxy groups of the peptides and peptide blocks, facilitating the purification of the peptides synthesized. After the elimination of the N- and C-terminal protective groups, the peptides were deblocked with 1 M trifluoromethanesulfonic acid in trifluoroacetic acid containing 10% of thioanisole and were purified by prepatative reversed-phase chromatography. Conjugates of the peptides synthesized with bovine serum albumin have been obtained.

Research Organization:
All-Union Scientific-Research Institute of Molecular Biology, Novosibirsk (USSR)
OSTI ID:
5244049
Journal Information:
Sov. J. Bioorg. Chem. (Engl. Transl.); (United States), Vol. 11:8; Other Information: Translated from Bioorganicheskaya Khim.; 11: No. 8, 1037-1047(Aug 1985)
Country of Publication:
United States
Language:
English

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