GTPase调节因子的动力学和细胞分析。

Nava Segev, Richard A Kahn
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引用次数: 1

摘要

调控gtp酶通常被描述为控制多种细胞过程的二元分子开关,包括但不限于第二信使的产生(例如cAMP和肌醇磷酸)、细胞内交通、细胞骨架组织和细胞增殖。GEF刺激剂和GAP抑制剂调节这些蛋白的核苷酸结合状态。由于gtp酶及其调控因子与人类疾病的相关性,它们构成了一个主要的治疗靶点。目前,关于GTPase调控因子的信息大多来自于结构分析。这种结构信息仅限于某些条件,并不一定反映特异性或生理活性。为了解决关于特异性和作用机制的问题,有必要对GTPase调节因子进行动力学和基于细胞的分析。在这里,我们比较了这两种方法在Arf和异源三聚体g蛋白调节的背景下。
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Kinetic and cell-based analyses of GTPase regulators.

Regulatory GTPases are often portrayed as binary molecular switches that control a wide range of cellular processes, including, but not limited to, the generation of second messengers (e.g., cAMP and inositol phosphates), intracellular traffic, cytoskeleton organization and cell proliferation. GEF stimulators and GAP inhibitors regulate the nucleotide-bound state of these proteins. Because of the relevance of GTPases and their regulators to human diseases, they comprise a major therapeutic target. Currently, most of the information about GTPase regulators comes from structure analyses. Such structural information is limited to certain conditions and does not necessarily reflect specificity or physiological activity. To address questions about specificity and mechanisms of action, kinetic and cell-based analyses of GTPase regulators is necessary. Here, we compare these two approaches in the context of regulators of Arf and heterotrimeric G-proteins.

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