Tubulin photoaffinity labeling study with a plinabulin chemical probe possessing a biotin tag at the oxazole

被引:25
作者
Yamazaki, Yuri [1 ]
Kido, Yui [1 ]
Hidaka, Koushi [2 ]
Yasui, Hiroyuki [3 ]
Kiso, Yoshiaki [2 ]
Yakushiji, Fumika [1 ]
Hayashi, Yoshio [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Dept Med Chem, Tokyo 1920392, Japan
[2] Kyoto Pharmaceut Univ, Ctr Frontier Res Med Sci, Dept Med Chem, Kyoto 6078412, Japan
[3] Kyoto Pharmaceut Univ, Dept Analyt & Bioinorgan Chem, Kyoto 6078414, Japan
关键词
Anti-cancer agent; Diketopiperazine; Phenylahistin; Tubulin; Vascular disrupting agent; IN-VITRO; BETA-TUBULIN; DERIVATIVES; AGENTS; PHENYLAHISTIN; DRUG; SITE; (-)-PHENYLAHISTIN; MICROTUBULES; BINDING;
D O I
10.1016/j.bmc.2010.10.055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new bioactive photoaffinity probe KPU-252-B1 (4) possessing a biotin tag on the oxazole ring of a potent plinabulin derivative KPU-244 (2) was synthesized via the Cu-I-catalyzed Huisgen's cycloaddition reaction to understand the precise binding mode of the diketopiperazine-based anti-microtubule agent plinabulin on tubulin. Probe 4 showed significant binding affinity toward tubulin and cytotoxicity against an HT-29 cells. A photoaffinity labeling study suggested that probe 4 specifically recognizes tubulin at a binding site that binds plinabulin or colchicine, most likely near or at the colchicine binding site, which is located at the interfacial region formed by alpha- and beta-tubulin association. The results also demonstrated that probe 4 may serve as a useful plinabulin chemical probe to investigate the molecular mechanism by which anti-microtubule diketopiperazine derivatives operate. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:595 / 602
页数:8
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