A High-Content, Cell-Based Screen Identifies Micropolyin, A New Inhibitor of Microtubule Dynamics

被引:11
作者
De Rycker, Manu [1 ]
Rigoreau, Laurent [2 ]
Dowding, Sarah [1 ]
Parker, Peter J. [1 ,3 ]
机构
[1] Canc Res UK, London Res Inst, Prot Phosphorylat Lab, London WC2A 3PX, England
[2] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
[3] Guys Hosp, New Hunts House, Div Canc Studies Kings Coll London, London SE1 1UL, England
关键词
cell cycle; chemical genetics; high-content screen; inhibitors; microtubule; CHEMICAL GENETICS; MITOTIC SPINDLE; CENTROMERE DYNAMICS; STRUCTURAL BASIS; NOCODAZOLE; TUBULIN; MOLECULES; DRUGS; VINBLASTINE; CHECKPOINT;
D O I
10.1111/j.1747-0285.2009.00817.x
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
High-content cell-based screens provide a powerful tool to identify new chemicals that interfere with complex biological processes. Here, we describe the identification of a new inhibitor of microtubule dynamics (micropolyin) using a high-content screen. Integrated high-resolution imaging allowed for fast selection of hits and progression to target identification. Treatment of cells with micropolyin efficiently causes a pro-metaphase arrest, with abnormal spindle morphology and with the spindle assembly checkpoint activated. The arrest appears to result from interference of micropolyin with microtubule dynamics. We show in vitro that tubulin is indeed the target of micropolyin and that micropolyin inhibits microtubule polymerization. Our results demonstrate the power of high-content image- and cell-based screening approaches to identify potential new drug candidates. As our approach is unbiased, it should allow for discovery of new targets that may otherwise be overlooked.
引用
收藏
页码:599 / 610
页数:12
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