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Ash/Grb2相互作用的GDP/GTP交换蛋白的动力学特性

Kinetic properties of Ash/Grb2-interacting GDP/GTP exchange protein.

作者信息

Nakanishi H, Orita S, Kaibuchi K, Miura K, Miki H, Takenawa T, Takai Y

机构信息

Department of Biochemistry, Kobe University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1994 Feb 15;198(3):1255-61. doi: 10.1006/bbrc.1994.1177.

Abstract

Ash/Grb2 is a protein having one SH2 domain flanked by two SH3 domains and is implicated to serve as an adaptor protein which links the EGF receptor to mammalian Sos (mSos), a GDP/GTP exchange protein for Ras. We isolated here several Ash-interacting proteins from bovine brain cytosol by use of glutathione-S-transferase-Ash-linked agarose column chromatography. The Ash-interacting proteins stimulated the GDP/GTP exchange reaction of Ki-Ras and Ha-Ras but not that of other small GTP-binding proteins including at least Rap1, RhoA, Rac1, and Rab3A. The Ash-interacting proteins were much more active on the post-translationally lipid-modified form of Ki-Ras than on the unmodified form. At least one of them was identified as mSos by Western blot analysis using a specific anti-mSos antibody.

摘要

Ash/Grb2是一种蛋白质,它有一个位于两个SH3结构域之间的SH2结构域,被认为作为衔接蛋白,将表皮生长因子受体与哺乳动物Sos(mSos)相连,mSos是一种Ras的GDP/GTP交换蛋白。我们在此通过使用谷胱甘肽-S-转移酶-Ash连接的琼脂糖柱色谱法,从牛脑细胞质中分离出了几种与Ash相互作用的蛋白质。这些与Ash相互作用的蛋白质刺激了Ki-Ras和Ha-Ras的GDP/GTP交换反应,但不刺激包括至少Rap1、RhoA、Rac1和Rab3A在内的其他小GTP结合蛋白的反应。与Ash相互作用的蛋白质对翻译后脂质修饰形式的Ki-Ras的活性比对未修饰形式的活性高得多。使用特异性抗mSos抗体的蛋白质印迹分析将其中至少一种鉴定为mSos。

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