Tag-Convertible Photocrosslinker with Click-On/Off N-Acylsulfonamide Linkage for Protein Identification

Ryuji Hayashi, Shota Morimoto, Takenori Tomohiro*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The N-acylsulfonamide group, known as a safety-catch linker, has been applied to photoaffinity labeling (PAL) using a cinnamate-type photocrosslinker to improve the efficiency of PAL-based target identification. A bioorthogonal sulfo-click reaction was used to stably link a photocrosslinker unit with N-acylsulfonamide linkage to produce a photoactivatable probe without any protection. In addition, the crosslinked protein was selectively isolated with a small cinnamate tag via linkage disruption upon N-alkylation. Furthermore, the tag moiety was photochemically converted to a stable coumarin derivative by losing a water molecule, which is a useful property in MS-based identification.

Original languageEnglish
Pages (from-to)3145-3148
Number of pages4
JournalChemistry - An Asian Journal
Volume14
Issue number18
DOIs
StatePublished - 2019/09/16

Keywords

  • cleavage
  • coumarin
  • fluorescence
  • photoaffinity labeling
  • sulfo-click reaction

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry

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