Protein Dynamics in Drug Combinations: a Linear Superposition of Individual-Drug Responses

被引:84
作者
Geva-Zatorsky, Naama [1 ,2 ]
Dekel, Erez [1 ,2 ]
Cohen, Ariel A. [1 ,2 ]
Danon, Tamar [1 ,2 ]
Cohen, Lydia [1 ,2 ]
Alon, Uri [1 ,2 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Phys Complex Syst, IL-76100 Rehovot, Israel
关键词
GENE NETWORKS; HUMAN-CELLS; SYSTEMS; PROTEOMICS; THERAPY; SYNERGY;
D O I
10.1016/j.cell.2010.02.011
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
Drugs and drug combinations have complex biological effects on cells and organisms. Little is known about how drugs affect protein dynamics that determine these effects. Here, we use a dynamic proteomics approach to accurately follow 15 protein levels in human cells in response to 13 different drugs. We find that protein dynamics in response to combinations of drugs are described accurately by a linear superposition ( weighted sum) of their response to individual drugs. The weights in this superposition describe the relative impact of each drug on each protein. Using these weights, we show that one can predict the dynamics in a three-drug or four-drug combination on the basis of the dynamics in drug pairs. Our approach might eliminate the need to increase the number of experiments exponentially with the number of drugs and suggests that it might be possible to rationally control protein dynamics with specific drug combinations.
引用
收藏
页码:643 / 651
页数:9
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