抄録
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.
本文言語 | 英語 |
---|---|
ページ(範囲) | 3145-3148 |
ページ数 | 4 |
ジャーナル | Chemistry - An Asian Journal |
巻 | 14 |
号 | 18 |
DOI | |
出版ステータス | 出版済み - 2019/09/16 |
ASJC Scopus 主題領域
- 生化学
- 有機化学