抄録
We employed a fluorescent substrate-based target discovery approach to screen the enzymome for metabolic activity towards pyruvyl-amidated peptides, and identified an acylamino acid-releasing enzyme (APEH). Cells overexpressing APEH exhibited higher metabolic activity towards the probe, N-pyruvyl-leucyl-7-amido-4-methylcoumarin (Pyr-Leu-AMC), while the selective APEH inhibitor AA74-1 blocked the reaction. Metabolism of various pyruvylated peptides in liver lysate was almost completely blocked by AA74-1. Pyruvyl peptides are synthesized in response to oxidative stress, but their biological role is poorly understood; identification of a key contributor to their metabolism should stimulate research on pathways leading from oxidative stress to protein modification and biological output.
本文言語 | English |
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ページ(範囲) | 4377-4380 |
ページ数 | 4 |
ジャーナル | Chemical Communications |
巻 | 52 |
号 | 23 |
DOI | |
出版ステータス | Published - 2016 |
外部発表 | はい |
ASJC Scopus subject areas
- 触媒
- 電子材料、光学材料、および磁性材料
- セラミックおよび複合材料
- 化学 (全般)
- 表面、皮膜および薄膜
- 金属および合金
- 材料化学