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Anti-microtubule ‘plinabulin’ chemical probe KPU-244-B3 labeled both α- and β-tubulin

Authors :
Yamazaki, Yuri
Sumikura, Makiko
Hidaka, Koushi
Yasui, Hiroyuki
Kiso, Yoshiaki
Yakushiji, Fumika
Hayashi, Yoshio
Source :
Bioorganic & Medicinal Chemistry. May2010, Vol. 18 Issue 9, p3169-3174. 6p.
Publication Year :
2010

Abstract

Abstract: Plinabulin (1, NPI-2358), a potent microtubule-targeting agent derived from the natural diketopiperazine ‘phenylahistin’ with a colchicine-like tubulin depolymerization activity, is an anticancer agent undergoing Phase II clinical trials in four countries including the United States. In order to understand the precise binding mode of plinabulin with tubulin, a new bioactive biotin-tagged photoaffinity probe 4 (KPU-244-B3) was designed and synthesized. Probe 4 showed significant binding affinity to tubulin in a binding assay, and selectively bound to tubulin in an HT-1080 cell lysate without photo-irradiation. In a tubulin photoaffinity labeling study, probe 4 labeled both α- and β-tubulin subunits and these interactions were competitively inhibited by plinabulin during photo-irradiation. These results suggest that plinabulin binds in the boundary region between α- and β-tubulin near the colchicine binding site, and not inside the colchicine binding cavity. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
09680896
Volume :
18
Issue :
9
Database :
Academic Search Index
Journal :
Bioorganic & Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
50357992
Full Text :
https://doi.org/10.1016/j.bmc.2010.03.037