In pursuit of carbohydrate-based HIV vaccines, Part 2: The total synthesis of high-mannose-type gp120 fragments-evaluation of strategies directed to maximal convergence
被引:102
作者:
Geng, XD
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机构:Sloan Kettering Inst Canc Res, Bioorgan Chem Lab, New York, NY 10021 USA
Geng, XD
Dudkin, VY
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机构:Sloan Kettering Inst Canc Res, Bioorgan Chem Lab, New York, NY 10021 USA
Dudkin, VY
Mandal, M
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机构:Sloan Kettering Inst Canc Res, Bioorgan Chem Lab, New York, NY 10021 USA
Mandal, M
Danishefsky, SJ
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机构:Sloan Kettering Inst Canc Res, Bioorgan Chem Lab, New York, NY 10021 USA
Danishefsky, SJ
机构:
[1] Sloan Kettering Inst Canc Res, Bioorgan Chem Lab, New York, NY 10021 USA
[2] Columbia Univ, Dept Chem, New York, NY 10027 USA
antigens;
glycoconjugates;
glycopeptides;
mannosylation;
total synthesis;
D O I:
10.1002/anie.200353626
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A layered approach" and a "block approach" were used to assemble the high-mannose glycan of gp120 glycopeptide fragments (e.g. high-mannose-type conjugates gp120316-3351). The glycan was then conjugated with the gp120 peptide segments through direct aspartylation."