Affinity Labeling with 4-Azidophthalimide (AzPI): Relation between Labeling Rate and Fluorescence Intensity

被引:5
作者
Chiba, Kosuke [1 ]
Hashimoto, Yuichi [1 ]
Yamaguchi, Takao [1 ,2 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, 1-1-1 Yayoi, Tokyo 1130032, Japan
[2] Osaka Univ, Grad Sch Pharmaceut Sci, 1-6 Yamadaoka, Suita, Osaka 5650871, Japan
基金
日本学术振兴会;
关键词
photoaffinity labeling; azidophthalimide; target identification; fluorescence; chemiluminescence; PHOTO-CROSS-LINKERS; IDENTIFICATION; CHEMISTRY; PROTEINS; TARGET; BINDING; CELLS;
D O I
10.1248/cpb.c17-00546
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We recently developed 4-azidophthalimide (AzPI) as a compact fluorogenic photoreactive tag that can be attached to ligands to achieve selective fluorescence labeling of target proteins even in the presence of a large excess of non-target proteins. To further establish the utility of the AzPI tag, we focused here on streptavidin labeling with biotin AzPI conjugates, and evaluated the relation between the amount of covalently labeled streptavidin (labeling rate) and fluorescence intensity. The labeling rate was proportional to the fluorescence intensity under standardized photo-irradiation conditions. Prolongation of the photo-irradiation time led to a marked increase in the labeling rate, but this was accompanied by a gradual decrease in the fluorescence intensity, which appeared to be due at least in part to photo-induced degradation of the target streptavidin. These findings should be helpful for achieving sensitive fluorescence detection of target proteins by using the AzPI tag.
引用
收藏
页码:994 / 996
页数:3
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