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

Youhei Sohma, Atsuhiko Taniguchi, Taku Yoshiya, Yousuke Chiyomori, Fukue Fukao, Setsuko Nakamura, Mariusz Skwarczynski, Takuma Okada, Keisuke Ikeda, Yoshio Hayashi, Tooru Kimura, Shun Hirota, Katsumi Matsuzaki, Yoshiaki Kiso*

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

25 被引用数 (Scopus)

抄録

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 β peptides in Alzheimer's disease, represents a valuable use of the isopeptide method in Chemical Biology-oriented research.

本文言語英語
ページ(範囲)823-828
ページ数6
ジャーナルJournal of Peptide Science
12
12
DOI
出版ステータス出版済み - 2006/12

ASJC Scopus 主題領域

  • 構造生物学
  • 生化学
  • 分子医療
  • 分子生物学
  • 薬理学
  • 創薬
  • 有機化学

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