Chemoenzymatic Synthesis of the Human CD52 and CD24 Antigen Analogues
被引:9
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作者:
Wu, Zhimeng
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Wayne State Univ, Dept Chem, Detroit, MI 48202 USAWayne State Univ, Dept Chem, Detroit, MI 48202 USA
Wu, Zhimeng
[1
]
Guo, Xueqing
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机构:
Wayne State Univ, Dept Chem, Detroit, MI 48202 USAWayne State Univ, Dept Chem, Detroit, MI 48202 USA
Guo, Xueqing
[1
]
Gu, Guofeng
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机构:
Shandong Univ, Natl Glycoengn Res Ctr, Jinan 250100, Peoples R ChinaWayne State Univ, Dept Chem, Detroit, MI 48202 USA
Gu, Guofeng
[2
]
Guo, Zhongwu
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机构:
Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
Shandong Univ, Natl Glycoengn Res Ctr, Jinan 250100, Peoples R ChinaWayne State Univ, Dept Chem, Detroit, MI 48202 USA
Guo, Zhongwu
[1
,2
]
机构:
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
[2] Shandong Univ, Natl Glycoengn Res Ctr, Jinan 250100, Peoples R China
Analogs of the human CD52 and CO24 antigens carrying the common core structure of glycosylphosphatidylinositol (GPI) anchors and the intact polypeptide sequences of CD52 and CD24 were chemoenzymatically synthesized. CD52 and CD24 proteins were obtained by solid-phase peptide synthesis and then coupled to chemically synthesized GPI anchors under the influence of a bacterial enzyme, sortase A, to afford the target molecules in good yields.