Small Molecule Probes of Cellular Pathways and Networks

被引:35
作者
Castoreno, Adam B.
Eggert, Ulrike S. [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Cytokinesis; High content screening; Network; Pathway; Profiling; Rho pathway; Small molecule probes; BCR-ABL; INHIBITORS; SCREEN; DISCOVERY; TARGETS; DRUGS; MODEL;
D O I
10.1021/cb1002976
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Small molecules are important not only as therapeutics to treat disease but also as chemical tools to probe complex biological processes. The discovery of novel bioactive small molecules has largely been catalyzed by screening diverse chemical libraries for alterations in specific activities in pure proteins assays or in generating cell-based phenotypes. New approaches are needed to close the vast gap between the ability to study either single proteins or whole cellular processes. This Review focuses on the growing number of studies aimed at understanding In more detail how small molecules perturb particular signaling pathways and larger networks to yield distinct cellular phenotypes. This type of pathway-level analysis and phenotypic profiling provides valuable insight into mechanistic action of small molecules and can reveal off-target effects and improve our understanding of how proteins within a pathway regulate signaling.
引用
收藏
页码:86 / 94
页数:9
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