利用X-Machines研究NF-κB信号通路中的IKK动态

R. Williams, J. Timmis, E. Qwarnstrom
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引用次数: 3

摘要

转录因子NF-κB是一种生物成分,对先天免疫系统相关基因的调节起着核心作用。已知该通路的失调与大量炎症性疾病有关。尽管自1986年发现以来进行了大量的研究,但我们仍然无法控制信号通路,从而限制NF-κB在促进炎症性疾病中的作用。我们开发了一种基于试剂的IL-1刺激的NF-κB信号通路模型,该模型已在单细胞水平上校准为湿实验室数据。通过严格的软件工程,我们相信我们的模型提供了底层真实世界系统的抽象视图,并且可以通过计算机实验用于预测能力。在这项研究中,我们主要关注IKK复合物的动力学及其对NF-κB的激活。我们基于主体的模型表明,该通路对以下因素敏感:IKK与受抑制的NF-κ b -κ b α复合物结合概率的变化;以及IKK的时间再结合延迟的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating IKK dynamics in the NF-κB signalling pathway using X-Machines
The transcription factor NF-κB is a biological component that is central to the regulation of genes involved in the innate immune system. Dysregulation of the pathway is known to be involved in a large number of inflammatory diseases. Although considerable research has been performed since its discovery in 1986, we are still not in a position to control the signalling pathway, and thus limit the effects of NF-κB within promotion of inflammatory diseases. We have developed an agent-based model of the IL-1 stimulated NF-κB signalling pathway, which has been calibrated to wet-lab data at the single-cell level. Through rigorous software engineering, we believe our model provides an abstracted view of the underlying real-world system, and can be used in a predictive capacity through in silico experimentation. In this study, we have focused on the dynamics of the IKK complex and its activation of NF-κB. Our agent-based model suggests that the pathway is sensitive to: variations in the binding probability of IKK to the inhibited NF-κB-IκBα complex; and variations in the temporal rebinding delay of IKK.
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