首页> 美国卫生研究院文献>Frontiers in Physiology >Research Topic: From structural to molecular systems biology: experimental and computational approaches to unravel mechanisms of kinase activity regulation in cancer and neurodegeneration: How scaffolds shape MAPK signaling: what we know and opportunities for systems approaches
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Research Topic: From structural to molecular systems biology: experimental and computational approaches to unravel mechanisms of kinase activity regulation in cancer and neurodegeneration: How scaffolds shape MAPK signaling: what we know and opportunities for systems approaches

机译:研究主题:从结构生物学到分子系统生物学:揭示癌症和神经变性中激酶活性调节机制的实验和计算方法:支架如何塑造MAPK信号传导:我们所知道的和系统方法的机会

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摘要

Scaffolding proteins add a new layer of complexity to the dynamics of cell signaling. Above their basic function to bring several components of a signaling pathway together, recent experimental research has found that scaffolds influence signaling in a much more complex way: scaffolds can exert some catalytic function, influence signaling by allosteric mechanisms, are feedback-regulated, localize signaling activity to distinct regions of the cell or increase pathway fidelity. Here we review experimental and theoretical approaches that address the function of two MAPK scaffolds, Ste5, a scaffold of the yeast mating pathway and KSR1/2, a scaffold of the classical mammalian MAPK signaling pathway. For the yeast scaffold Ste5, detailed mechanistic models have been valuable for the understanding of its function. For scaffolds in mammalian signaling, however, models have been rather generic and sketchy. For example, these models predicted narrow optimal scaffold concentrations, but when revisiting these models by assuming typical concentrations, rather a range of scaffold levels optimally supports signaling. Thus, more realistic models are needed to understand the role of scaffolds in mammalian signal transduction, which opens a big opportunity for systems biology.
机译:支架蛋白为细胞信号传导的动力学增加了新的复杂性。除了将信号传导途径的几个组成部分整合在一起的基本功能外,最近的实验研究还发现,支架以更复杂的方式影响信号传导:支架可以发挥某些催化功能,通过变构机制影响信号传导,受到反馈调节,定位信号传导对细胞不同区域的活性或增加途径保真度。在这里,我们审查实验和理论方法,以解决两个MAPK支架,Ste5,酵母交配途径的支架和KSR1 / 2,经典哺乳动物MAPK信号通路的支架的功能。对于酵母支架Ste5,详细的机理模型对于理解其功能非常有价值。然而,对于哺乳动物信号传导中的支架,模型已经相当通用和粗略了。例如,这些模型预测了狭窄的最佳支架浓度,但是当通过假设典型浓度重新访问这些模型时,则一定范围的支架水平最佳地支持信号传导。因此,需要更现实的模型来了解支架在哺乳动物信号转导中的作用,这为系统生物学打开了一个巨大的机会。

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