Glycotentacles: Synthesis of cyclic glycopeptides, toward a tailored blocker of influenza virus hemagglutinin

被引:74
作者
Ohta, T
Miura, N
Fujitani, N
Nakajima, F
Niikura, K
Sadamoto, R
Guo, CT
Suzuki, T
Suzuki, Y
Monde, K
Nishimura, SI
机构
[1] Hokkaido Univ, Frontier Res Ctr Postgenom Sci & Technol, Grad Sch Sci, Div Biol Sci, Sapporo, Hokkaido 0010021, Japan
[2] Univ Shizuoka, Sch Pharmaceut Sci, Dept Biochem, Shizuoka 4428526, Japan
[3] AIST, Sapporo, Hokkaido 0628517, Japan
关键词
carbohydrates; glycopeptides; influenza viruses; inhibitors; protein design;
D O I
10.1002/anie.200351640
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Blocking flu: A cyclic peptide, cyclo(Ser-Gly-Gly-Gln-Ser-His-Asp) 3, is an excellent scaffold for the synthesis of a cyclic glycopeptide carrying GM3 oligosaccharides with a potent inhibitory effect on the hemagglutination induced by the influenza virus. Tridentate binding of the gylcopeptide is shown to produce a much greater inhibitory effect than di- or monodentate binding. The shape of the glycopeptide protein scaffold, which is determined by the amino acid sequence employed, is also found to be significant in determining the inhibitory activity.
引用
收藏
页码:5186 / 5189
页数:4
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