gpcr / gef激活多个gtpase的信号放大模型是否与广谱异源三聚体和RAS超家族gtpase相关?

Cellular logistics Pub Date : 2014-05-01 eCollection Date: 2014-06-01 DOI:10.4161/21592780.2014.943602
Richard A Kahn
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引用次数: 4

摘要

生物过程的概念或模型塑造了我们如何思考、讨论它们,以及设计实验来测试它们的各个方面。由于我们通过调节gtpase建立细胞信号传导模型的重要性以及将这些模型扩展到相关信号传导模块的愿望,我在整个职业生涯中一直着迷于异源三聚体G蛋白和单体RAS超家族gtpase建模之间的异同。最近与同事的讨论使我得出结论,研究人员在如何模拟单体和三聚体gtp酶的激活和信号传递过程方面存在越来越大的分歧,而且每个阵营都令人惊讶地缺乏共识。本系列文章是对这些讨论的回应,旨在引发新的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Is the model of signal amplification by GPCRs/GEFs activating multiple GTPases relevant to a broad spectrum of heterotrimeric and RAS superfamily GTPases?

Is the model of signal amplification by GPCRs/GEFs activating multiple GTPases relevant to a broad spectrum of heterotrimeric and RAS superfamily GTPases?

Is the model of signal amplification by GPCRs/GEFs activating multiple GTPases relevant to a broad spectrum of heterotrimeric and RAS superfamily GTPases?

Concepts or models of biological processes shape how we think about them, discuss them, and design experiments to test aspects of them. Because of the importance of our models of cell signaling by regulatory GTPases and the desire to extend those models to related signaling modules, I have throughout my career been fascinated by the similarities and differences between the modeling of heterotrimeric G protein and monomeric RAS superfamily GTPases. Recent discussions with colleagues led me to conclude that there is a growing divergence in how researchers model the activation and signaling processes of monomeric and trimeric GTPases and also a surprising lack of consensus within each camp. This series of articles arose in response to these discussions and is intended to spark new ones.

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