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[胃肠道-PIX蛋白复合物:ARF及Rac/Cdc42 GTP酶的枢纽]

[The GIT-PIX protein complex: a hub to ARF and Rac/Cdc42 GTPases].

作者信息

Zeniou-Meyer Maria, Borg Jean-Paul, Vitale Nicolas

机构信息

CNRS UPR-2356, Neurotransmission et sécrétion neuroendocrine, Centre de neurochimie, Strasbourg, France.

出版信息

Med Sci (Paris). 2005 Oct;21(10):849-53. doi: 10.1051/medsci/20052110849.

Abstract

We recently described that the tumor suppressor factor Scribble anchors the PIX exchange factor for Rac/Cdc42 and the ARF-GAP GIT proteins at the plasma membrane. Because it has been postulated that the GIT-PIX proteins dimerize and tightly self-assemble to form a high molecular weight complex, this nexus may be capable of linking together important signalling molecules to control cytosqueleton polymerization and membrane dynamics. To date, most studies that have tempted to unravel the function of these proteins have found their implication in a great variety of cellular functions (receptor recycling, endo-exocytosis, cell migration, synapse formation...) but have mostly neglected to consider the multimeric organization of this hub. There is no doubt that our comprehension of physiopathological disorders such as cancers will be improved when the nature of the complex pathways integrated by the GIT-PIX nodule will be understood.

摘要

我们最近描述了肿瘤抑制因子Scribble在质膜上锚定Rac/Cdc42的PIX交换因子和ARF-GAP GIT蛋白。由于据推测GIT-PIX蛋白会二聚化并紧密自组装形成高分子量复合物,这个连接点可能能够将重要的信号分子连接在一起,以控制细胞骨架聚合和膜动力学。迄今为止,大多数试图阐明这些蛋白质功能的研究都发现它们参与了多种细胞功能(受体循环、胞吞胞吐、细胞迁移、突触形成……),但大多忽略了考虑这个枢纽的多聚体组织。毫无疑问,当我们理解了由GIT-PIX结节整合的复杂通路的本质时,我们对诸如癌症等生理病理紊乱的理解将会得到改善。

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