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小 GTP 酶信号转导和药理学中的蛋白质-膜相互作用:来自 Arf GTPases 研究的观点。

Protein-membrane interactions in small GTPase signalling and pharmacology: perspectives from Arf GTPases studies.

机构信息

CNRS, Ecole normale supérieure Paris-Saclay and Université Paris-Saclay, Gif-sur-Yvette, France.

出版信息

Biochem Soc Trans. 2020 Dec 18;48(6):2721-2728. doi: 10.1042/BST20200482.

Abstract

Small GTPases, in association with their GEFs, GAPs and effectors, control major intracellular processes such as signal transduction, cytoskeletal dynamics and membrane trafficking. Accordingly, dysfunctions in their biochemical properties are associated with many diseases, including cancers, diabetes, infections, mental disorders and cardiac diseases, which makes them attractive targets for therapies. However, small GTPases signalling modules are not well-suited for classical inhibition strategies due to their mode of action that combines protein-protein and protein-membrane interactions. As a consequence, there is still no validated drug available on the market that target small GTPases, whether directly or through their regulators. Alternative inhibitory strategies are thus highly needed. Here we review recent studies that highlight the unique modalities of the interaction of small GTPases and their GEFs at the periphery of membranes, and discuss how they can be harnessed in drug discovery.

摘要

小分子 GTPases 与其 GEFs、GAPs 和效应物一起,控制着信号转导、细胞骨架动态和膜运输等主要的细胞内过程。因此,它们生化特性的功能障碍与许多疾病有关,包括癌症、糖尿病、感染、精神障碍和心脏病,这使得它们成为治疗的有吸引力的靶点。然而,由于其作用模式结合了蛋白-蛋白和蛋白-膜相互作用,小分子 GTPases 信号转导模块不适合传统的抑制策略。因此,目前市场上还没有针对小分子 GTPases 的经过验证的药物,无论是直接针对小分子 GTPases 还是通过其调节剂。因此,非常需要替代的抑制策略。在这里,我们回顾了最近的研究,这些研究强调了小分子 GTPases 及其在膜边缘的 GEFs 的相互作用的独特模式,并讨论了如何在药物发现中利用这些模式。

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