Prigmore E, Ahmed S, Best A, Kozma R, Manser E, Segal A W, Lim L
Department of Neurochemistry, Institute of Neurology, London, United Kingdom.
J Biol Chem. 1995 May 5;270(18):10717-22. doi: 10.1074/jbc.270.18.10717.
Cdc42Hs and Rac1 are members of the Ras superfamily of small molecular weight (p21) GTP binding proteins. Cdc42Hs induces filopodia formation in Swiss 3T3 fibroblasts while Rac1 induces membrane ruffling. Rac1 also activates superoxide production by the components (cytochrome b, p40phox, p67phox, and p47phox) of the neutrophil oxidase. To isolate target proteins involved in these signaling pathways, we have probed proteins from neutrophil cytosol immobilized on nitrocellulose with Cdc42Hs labeled with [gamma-32P]GTP. Cdc42Hs probe detected binding protein(s) of 66-68 kDa in neutrophil cytosol. Rac1 probe also detected the 66-68-kDa proteins, suggesting the possibility that p67phox may be a binding protein for both of these p21 proteins. Indeed, Cdc42Hs and Rac1 were found to bind specifically to purified recombinant p67phox but not the other oxidase components. A 68-kDa Cdc42Hs binding protein was purified from neutrophil cytosol and found to be related to the recently described p65pak kinase from brain. These results suggest that the p68 kinase and p67phox are targets for Cdc42Hs and Rac1 in neutrophils.
Cdc42Hs和Rac1是小分子量(p21)GTP结合蛋白的Ras超家族成员。Cdc42Hs可诱导瑞士3T3成纤维细胞中丝状伪足的形成,而Rac1可诱导膜皱襞的形成。Rac1还可激活中性粒细胞氧化酶的组分(细胞色素b、p40phox、p67phox和p47phox)产生超氧化物。为了分离参与这些信号通路的靶蛋白,我们用[γ-32P]GTP标记的Cdc42Hs探测固定在硝酸纤维素上的中性粒细胞胞质溶胶中的蛋白。Cdc42Hs探针在中性粒细胞胞质溶胶中检测到了66 - 68 kDa的结合蛋白。Rac1探针也检测到了66 - 68 kDa的蛋白,这表明p67phox可能是这两种p21蛋白的结合蛋白。事实上,发现Cdc42Hs和Rac1能特异性结合纯化的重组p67phox,而不与其他氧化酶组分结合。从中性粒细胞胞质溶胶中纯化出一种68 kDa的Cdc42Hs结合蛋白,发现它与最近报道的来自大脑的p65pak激酶有关。这些结果表明,p68激酶和p67phox是中性粒细胞中Cdc42Hs和Rac1的靶标。