Intact glycation end products containing carboxymethyl-lysine and glyoxal lysine dimer obtained from synthetic collagen model peptide

被引:14
作者
Yamada, H
Sasaki, T
Niwa, S
Oishi, T
Murata, M
Kawakami, T
Aimoto, S
机构
[1] Osaka Univ, Grad Sch Sci, Dept Chem, Toyonaka, Osaka 5600043, Japan
[2] Osaka Univ, Inst Prot Res, Suita, Osaka 5650871, Japan
关键词
advanced glycation end products; collagen;
D O I
10.1016/j.bmcl.2004.08.044
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Advanced glycation end products (AGE) are accumulated in human tissues when long-lived proteins are glycated due to hyperglycemia and/or aging. In this study, we synthesized a collagen model peptide, Ac-(Pro-Hyp-Gly)(5)-Pro-Lys-Gly-(Pro-Hyp-Gly)(5)-Ala-NH2 to investigate intact AGEs in peptides. The peptide formed a stable triple helix structure, and was subjected to glycation reactions with glucose, ribose and glyoxal. Besides carboxymethyl-lysine in the peptide, a conjugated form linked with glyoxal lysine dimer (GOLD) was detected upon treatment with glyoxal. This is the first example of intact glycation-derived dimers of peptides retaining intrinsic protein structures. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5677 / 5680
页数:4
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