Novel biotin linker with alkyne and amino groups for chemical labelling of a target protein of a bioactive small molecule

被引:8
作者
Anabuki, Tomoaki [1 ]
Tsukahara, Miu [1 ]
Okamoto, Masanori [2 ]
Matsuura, Hideyuki [1 ]
Takahashi, Kosaku [1 ]
机构
[1] Hokkaido Univ, Res Fac Agr, Kita Ku, Kita9 Nishi9, Sapporo, Hokkaido 0608589, Japan
[2] Utsunomiya Univ, Ctr Biosci Res & Educ, 350 Mine Cho, Utsunomiya, Tochigi 3218505, Japan
基金
日本学术振兴会;
关键词
Target protein identification; Crick reaction; Abscisic acid; PYL; TERMINAL ALKYNES; PHOTOAFFINITY; CYCLOADDITION; PLANTS; AZIDES;
D O I
10.1016/j.bmcl.2017.12.055
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We synthesized a novel linker (1) with biotin, alkyne and amino groups for the identification of target proteins using a small molecule that contains an azide group (azide probe). The alkyne in the linker bound the azide probe via an azide-alkyne Huisgen cycloaddition. A protein cross-linker effectively bound the conjugate of the linker and an azide probe with a target protein. The covalently bound complex was detected by western blotting. Linker 1 was applied to a model system using an abscisic acid receptor, RCAR/PYR/PYL (PYL). Cross-linked complexes of linker 1, the azide probes and the target proteins were successfully visualized by western blotting. This method of target protein identification was more effective than a previously developed method that uses a second linker with biotin, alkyne, and benzophenone (linker 2) that acts to photo-crosslink target proteins. The system developed in this study is a method for identifying the target proteins of small bioactive molecules and is different from photo-affinity labelling. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:783 / 786
页数:4
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