Simple and versatile method for tagging phenyldiazirine photophores

Hiroyuki Nakashima, Makoto Hashimoto, Yutaka Sadakane, Takenori Tomohiro, Yasumaru Hatanaka*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

The first effective method for the introduction of a versatile substituent on 3-phenyl-3-trifluoromethyldiazirine has been developed. The simple preparation of a useful aldehyde intermediate allows easy access to various elaborated photoaffinity ligands, including a l-phenylalanine analog bearing a diazirine ring (TmdPhe). The asymmetric synthesis of TmdPhe was easily accomplished in gram quantities. Site-directed incorporation of this compound into the structure of a calmodulin-binding peptide using automated peptide synthesis afforded a photoreactive peptide that was successfully used for the specific labeling of calmodulin.

Original languageEnglish
Pages (from-to)15092-15093
Number of pages2
JournalJournal of the American Chemical Society
Volume128
Issue number47
DOIs
StatePublished - 2006/11/29

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Biochemistry
  • Colloid and Surface Chemistry

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