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Screening for cell migration inhibitors via automated microscopy reveals a rho-kinase inhibitor
被引:108
|作者:
Yarrow, JC
[1
]
Totsukawa, G
Charras, GT
Mitchison, TJ
机构:
[1] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Inst Chem & Cell Biol, Boston, MA 02115 USA
[3] Rutgers State Univ, Dept Mol Biol & Biochem, Piscataway, NJ 08854 USA
来源:
关键词:
D O I:
10.1016/j.chembiol.2005.01.015
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:
Small-molecule kinase inhibitors are predominantly discovered in pure protein assays. We have discovered an inhibitor of Rho-kinase (ROCK) through an image-based, high-throughput screen of cell monolayer wound healing. Using automated microscopy, we screened a library of 16,000 compounds finding many that affected cell migration or cell morphology as well as compounds that blocked mitotic progression. We tested 200 compounds in a series of subassays and chose one, 3-(4-pyridyl)indole (Rockout), for more detailed characterization. Rockout inhibits blebbing and causes dissolution of actin stress fibers, phenocopying Rho-kinase inhibitors. Testing Rho-kinase activity in vitro, Rockout inhibits with an IC50 of 25 mu M (5-fold less potent than Y-27632) but has a similar specificity profile. We also profile the wound healing assay with a library of compounds with known bioactivities, revealing multiple pathways involved in the biology.
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页码:385 / 395
页数:11
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