Glycopolypeptides via Living Polymerization of Glycosylated-L-lysine N-Carboxyanhydrides

被引:147
作者
Kramer, Jessica R. [1 ]
Deming, Timothy J. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
关键词
RING-OPENING POLYMERIZATION; C-GLYCOSIDE ANALOG; BLOCK-COPOLYMERS; SIDE-CHAIN; ICE RECRYSTALLIZATION; POLYPEPTIDE VESICLES; 1ST SYNTHESIS; GLYCOPEPTIDE; CONFORMATION; BINDING;
D O I
10.1021/ja107425f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The preparation of new glycosylated-L-lysine-N-carboxyanhydride (glyco-K NCA) monomers is described. These monomers employ C-linked sugars and amide linkages to lysine for improved stability without sacrificing biochemical properties. Three glyco-K NCAs were synthesized, purified, and found to undergo living polymerization using transition metal initiation. These are the first living polymerizations of glycosylated NCAs and were used to prepare well-defined, high molecular weight glycopolypeptides and block and statistical glycocopolypeptides. This methodology solves many long-standing problems in the direct synthesis of glycopolypeptides from N-carboxyanhydrides relating to monomer synthesis, purification, and polymerization and gives polypeptides with 100% glycosylation. These long chain glycopolypeptides have potential to be good mimics of natural high molecular weight glycoproteins.
引用
收藏
页码:15068 / 15071
页数:4
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