From large networks to small molecules

被引:83
作者
Sharom, JR
Bellows, DS
Tyers, M
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M4G 1A8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/j.cbpa.2003.12.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Large-scale analysis of genetic and physical interaction networks has begun to reveal the global organization of the cell. Cellular phenotypes observed at the macroscopic level depend on the collective characteristics of protein and genetic interaction networks, which exhibit scale-free properties and are highly resistant to perturbation of a single node. The nascent field of chemical genetics promises a host of small-molecule probes to explore these emerging networks. Although the robust nature of cellular networks usually resists the action of single agents, they may be susceptible to rationally designed combinations of small molecules able to collectively shift network behavior.
引用
收藏
页码:81 / 90
页数:10
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