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Modulating protein-protein interaction networks in protein homeostasis

机译:调节蛋白质 - 蛋白质蛋白质相互作用网络

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摘要

Protein-protein interactions (PPIs) occur in complex networks. These networks are highly dependent on cellular context and can be extensively altered in disease states such as cancer and viral infection. In recent years, there has been significant progress in developing inhibitors that target individual PPIs either orthosterically (at the interface) or allosterically. These molecules can now be used as tools to dissect PPI networks. Here, we review recent examples that highlight the use of small molecules and engineered proteins to probe PPIs within the complex networks that regulate protein homeostasis. Researchers have discovered multiple mechanisms to modulate PPIs involved in host/viral interactions, deubiquitinases, the ATPase p97NCP, and HSP70 chaperones. However, few studies have evaluated the effect of such modulators on the target's network or have compared the biological implications of different modulation strategies. Such studies will have an important impact on next generation therapeutics.
机译:蛋白质 - 蛋白质相互作用(PPI)发生在复杂网络中。这些网络高度依赖于细胞背景,并且可以在诸如癌症和病毒感染的疾病状态中广泛改变。近年来,在显影靶向单独的PPI的抑制剂(在界面)或构成构造方向上存在显着进展。这些分子现在可以用作解剖PPI网络的工具。在这里,我们审查了最近的例子,突出了使用小分子和工程化蛋白在调节蛋白质稳态的复杂网络中探测PPI。研究人员已经发现了多种机制来调节宿主/病毒相互作用,脱硫酶,ATP酶P97NCP和HSP70伴侣的PPI。然而,很少有研究已经评估了这种调制器对目标网络的影响,或者已经比较了不同调制策略的生物学意义。这些研究将对下一代治疗剂产生重要影响。

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