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 language | English |
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Pages (from-to) | 3145-3148 |
Number of pages | 4 |
Journal | Chemistry - An Asian Journal |
Volume | 14 |
Issue number | 18 |
DOIs | |
State | Published - 2019/09/16 |
Keywords
- cleavage
- coumarin
- fluorescence
- photoaffinity labeling
- sulfo-click reaction
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry