Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Cell. 2010 Mar 5;140(5):643-51. doi: 10.1016/j.cell.2010.02.011.
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.
药物和药物组合对细胞和生物体具有复杂的生物学效应。目前人们对于药物如何影响决定这些效应的蛋白质动力学知之甚少。在这里,我们使用动态蛋白质组学方法来准确跟踪 13 种不同药物作用于人类细胞时的 15 种蛋白质水平。我们发现,药物组合作用于蛋白质的动力学可以通过其对单个药物的反应的线性叠加(加权和)来准确描述。该叠加中的权重描述了每种药物对每种蛋白质的相对影响。利用这些权重,我们表明可以根据药物对的动力学来预测三药或四药组合的动力学。我们的方法可能会消除随着药物数量呈指数级增加实验数量的必要性,并表明使用特定药物组合可能可以合理地控制蛋白质动力学。