Stein E, Cerretti D P, Daniel T O
Departments of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
J Biol Chem. 1996 Sep 20;271(38):23588-93. doi: 10.1074/jbc.271.38.23588.
ELK is a member of the Eph-related tyrosine kinase family that includes receptors signaling axonal guidance, neuronal bundling, and angiogenesis. We recently identified ELK expression in human renal microvascular endothelial cells and sought to identify intracellular proteins through which it signals responses. The cytoplasmic domain of ELK was used as "bait" in a yeast two-hybrid screen to identify interactive proteins expressed from a randomly primed embryonic murine library (E9.5-10.5). Among interactive products of 76 cDNAs characterized, 10 nonidentical, overlapping clones encoded the SH2 domain of the recently reported Grb10 adapter protein, and an additional 3 encoded Grb2. A self-phosphorylated recombinant, baculovirus-expressed GST-ELKcy fusion protein bound Grb10 and Grb2 from human renal microvascular endothelial cell extracts, while the unphosphorylated fusion form did not. Site-directed mutation identified Tyr-929 as a putative phosphorylation site required for Grb10, but not Grb2, interaction in yeast and recombinant protein assays. The ELK ligand, LERK-2/Fc, stimulated tyrosine phosphorylation of ELK, and recruitment of Grb10 and Grb2 to endothelial ELK receptors recovered by wheat germ agglutinin lectin and immunoprecipitation. These findings define ligand-activated interaction between ELK and the SH2 domains of Grb2 and the newly identified Grb10 protein that shares homology with a Caenorhabditis elegans gene product implicated in neural cell migration.
ELK是Eph相关酪氨酸激酶家族的成员,该家族包括参与轴突导向、神经元成束和血管生成信号传导的受体。我们最近在人肾微血管内皮细胞中鉴定出ELK的表达,并试图鉴定其通过哪些细胞内蛋白发出反应信号。在酵母双杂交筛选中,ELK的胞质结构域被用作“诱饵”,以鉴定从随机引发的胚胎小鼠文库(E9.5 - 10.5)中表达的相互作用蛋白。在76个经鉴定的cDNA相互作用产物中,10个不同的重叠克隆编码了最近报道的Grb10衔接蛋白的SH2结构域,另外3个编码Grb2。一种自磷酸化的重组杆状病毒表达的GST - ELKcy融合蛋白能与人肾微血管内皮细胞提取物中的Grb10和Grb2结合,而未磷酸化的融合形式则不能。定点突变确定Tyr - 929是酵母和重组蛋白分析中Grb10(而非Grb2)相互作用所需的假定磷酸化位点。ELK配体LERK - 2/Fc刺激ELK的酪氨酸磷酸化,并通过麦胚凝集素和免疫沉淀将Grb10和Grb2募集到内皮ELK受体上。这些发现确定了ELK与Grb2的SH2结构域以及新鉴定的Grb10蛋白之间的配体激活相互作用,Grb10与秀丽隐杆线虫中一个与神经细胞迁移有关的基因产物具有同源性。