"Examining RAS pathway rewiring with a chemically inducible activator of RAS".

Q2 Biochemistry, Genetics and Molecular Biology Small GTPases Pub Date : 2020-11-01 Epub Date: 2018-04-10 DOI:10.1080/21541248.2018.1446697
John C Rose, Emily M Dieter, Daniel Cunningham-Bryant, Dustin J Maly
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引用次数: 4

Abstract

RAS signaling pathways govern diverse cellular processes, are dynamic, and exhibit marked plasticity. Yet, these features also present a considerable obstacle to their study. Here, we report the use of a recently described RAS rheostat, Chemically Inducible Activator of RAS (CIAR), to study two poorly understood phenomena in RAS biology. First, we show that short-term activation of wild type endogenous RAS can desensitize cells to EGF stimulation. Second, we examine the phenomena of paradoxical activation of RAS/ERK signaling by RAF inhibitors. Specifically, we characterize the effects on RAS/ERK signaling kinetics of four RAF inhibitors, which stabilize distinct ATP-binding site conformations. These results demonstrate the utility of CIAR in conducting quantitative studies of complex features of RAS biology.

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“用化学诱导的RAS激活剂检测RAS通路重新布线”。
RAS信号通路控制着不同的细胞过程,是动态的,并表现出显著的可塑性。然而,这些特征也给它们的研究带来了相当大的障碍。在这里,我们报告使用最近描述的RAS变阻器,化学诱导的RAS激活器(CIAR),来研究RAS生物学中两个鲜为人知的现象。首先,我们发现野生型内源性RAS的短期激活可以使细胞对EGF刺激脱敏。其次,我们研究了RAF抑制剂对RAS/ERK信号的矛盾激活现象。具体来说,我们描述了四种RAF抑制剂对RAS/ERK信号动力学的影响,这些抑制剂稳定了不同的atp结合位点构象。这些结果证明了CIAR在进行RAS生物学复杂特征定量研究中的实用性。
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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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