'Click peptide':: a novel 'O-acyl isopeptide method' for peptide synthesis and chemical biology-oriented synthesis of amyloid β peptide analogues

被引:23
作者
Sohma, Youhei
Taniguchi, Atsuhiko
Yoshiya, Taku
Chiyomori, Yousuke
Fukao, Fukue
Nakamura, Setsuko
Skwarczynski, Mariusz
Okada, Takuma
Ikeda, Keisuke
Hayashi, Yoshio
Kimura, Tooru
Hirota, Shun
Matsuzaki, Katsumi
Kiso, Yoshiaki [1 ]
机构
[1] Kyoto Pharmaceut Univ, Ctr Frontier Res Med Sci, Dept Med Chem, Century COE Program 21st,Yamashina Ku, Kyoto 6078412, Japan
[2] Kyoto Pharmaceut Univ, Dept Phys Chem, Century COE Program 21st, Kyoto 6078412, Japan
[3] PRESTO, JST, Kawaguchi, Saitama 3320012, Japan
[4] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
关键词
O-acyl isopeptide method; Alzheimer's disease; amyloid beta peptide; click peptide; difficult sequence;
D O I
10.1002/psc.817
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
After over a decade of studies on aspartic protease inhibitors and water-soluble prodrugs, we have been developing a novel method, since 2003, called 'O-acyl isopeptide method', for the synthesis of peptides containing difficult sequences. With our recent discoveries of 'O-acyl isodipeptide unit' and the 'racemization-free segment condensation method', this method has further evolved as a general synthetic method for peptides. Moreover, 'Click Peptide', which could be a powerful tool for identifying the pathological functions of amyloid beta peptides in Alzheimer's disease, represents a valuable use of the isopeptide method in Chemical Biology-oriented research. Copyright (c) 2006 European Peptide Society and John Wiley & Sons, Ltd.
引用
收藏
页码:823 / 828
页数:6
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