Synthesis and CD structural studies of CD52 peptides and glycopeptides

被引：8

作者：

Swarts, Benjamin M. ^{[1
]}

Chang, Yu-Cheng ^{[1
]}

Hu, Honggang ^{[1
]}

Guo, Zhongwu ^{[1
]}

机构：

[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA

来源：

CARBOHYDRATE RESEARCH | 2008年 / 343卷 / 17期

基金：

美国国家科学基金会;

关键词：

CD52; Peptide; Glycopeptide; N-Glycosylation; Circular dichroism (CD); Solid phase synthesis;

D O I：

10.1016/j.carres.2008.08.024

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The syntheses of five natural and N-terminal acetylated peptides and glycopeptides of the CD52 antigen are described. Solid phase peptide synthesis was employed in the construction of the target compounds from Fmoc-protected commercial amino acids and synthetic glycan-asparagine conjugates. Circular dichroism studies of the synthetic targets showed that they exist as random coils in solution, and no significant change in secondary structure was observed when the CD52 peptide was either acetylated at the N-terminus or glycosylated at the Asn(3) residue with a disaccharide or a fucose-containing branched trisaccharide. (C) 2008 Elsevier Ltd. All rights reserved,

引用

页码：2894 / 2902

页数：9

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