Title of article
Intact glycation end products containing carboxymethyl-lysine and glyoxal lysine dimer obtained from synthetic collagen model peptide
Author/Authors
Hiroaki Yamada، نويسنده , , Tomoko Sasaki Takayama، نويسنده , , Sachiko Niwa، نويسنده , , Tohru Oishi، نويسنده , , Michio Murata، نويسنده , , Toru Kawakami، نويسنده , , Saburo Aimoto and Yoshifumi Nishimura، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
4
From page
5677
To page
5680
Abstract
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.
Keywords
Advanced glycation end products , Collagen.* Corresponding author. Tel./fax: +81 66850 5774 , e-mail: murata@ch.wani.osaka-u.ac.jp
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2004
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
795046
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