期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 131, 期 15, 页码 5438-5443出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja808707w
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资金
- National Institutes of Health [CA28824]
- National Cancer Institute [T32 CA062948]
The Ala(1)-Gly(28) glycopeptide fragment (28) of EPO was prepared by chemical synthesis as a single glycoform. Key steps in the synthesis include attachment of a complex dodecasaccharide (7) to a seven amino acid peptide via Lansbury aspartylation, native chemical ligation to join peptide 19 with the glycopeptide domain 18, and a selective desulfurization at the ligation site to reveal the natural Ala(19). This glycopeptide fragment (28) contains both the requisite N-linked dodecasaccharide and a C-terminal (alpha)thioester handle, the latter feature permitting direct coupling with a glycopeptide fragment bearing N-terminal Cys(29) without further functionalization.
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