Rivero-Lezcano O M, Marcilla A, Sameshima J H, Robbins K C
Laboratory of Cellular Development and Oncology, National Institute of Dental Research, Bethesda, Maryland 20892-4330, USA.
Mol Cell Biol. 1995 Oct;15(10):5725-31. doi: 10.1128/MCB.15.10.5725.
In the second of a series of experiments designed to identify p47nck-Src homology 3 (SH3)-binding molecules, we report the cloning of SAKAP II (Src A box Nck-associated protein II) from an HL60 cDNA expression library. This molecule has been identified as a cDNA encoding the protein product of WASP, which is mutated in Wiskott-Aldrich syndrome patients. Studies in vivo and in vitro demonstrated a highly specific interaction between the SH3 domains of p47nck and Wiskott-Aldrich syndrome protein. Furthermore, anti-Wiskott-Aldrich syndrome protein antibodies recognized a protein of 66 kDa by Western blot (immunoblot) analysis. In vitro translation studies identified the 66-kDa protein as the protein product of WASP, and subcellular fractionation experiments showed that p66WASP is mainly present in the cytosol fraction, although significant amounts are also present in membrane and nuclear fractions. The main p47nck region implicated in the association with p66WASP was found to be the carboxy-terminal SH3 domain.
在旨在鉴定p47nck-Src同源结构域3(SH3)结合分子的系列实验的第二个实验中,我们报道了从HL60 cDNA表达文库中克隆出SAKAP II(Src A盒Nck相关蛋白II)。该分子已被鉴定为编码WASP蛋白产物的cDNA,WASP在威斯科特-奥尔德里奇综合征患者中发生突变。体内和体外研究表明,p47nck的SH3结构域与威斯科特-奥尔德里奇综合征蛋白之间存在高度特异性相互作用。此外,抗威斯科特-奥尔德里奇综合征蛋白抗体通过蛋白质印迹(免疫印迹)分析识别出一种66 kDa的蛋白质。体外翻译研究确定该66 kDa蛋白质为WASP的蛋白质产物,亚细胞分级分离实验表明,p66WASP主要存在于胞质溶胶部分,尽管在膜和核部分也有大量存在。发现与p66WASP结合的主要p47nck区域是羧基末端SH3结构域。