Huber L A, Ullrich O, Takai Y, Lütcke A, Dupree P, Olkkonen V, Virta H, de Hoop M J, Alexandrov K, Peter M
European Molecular Biology Laboratory, Cell Biology Programme, Heidelberg, Germany.
Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):7874-8. doi: 10.1073/pnas.91.17.7874.
For identification of Rab, Rac, Rho, Ral, Rap, and Arf proteins on two-dimensional polyacrylamide gels, we have expressed full-length cDNAs of members of these protein families with the T7 RNA polymerase-recombinant vaccinia virus expression system. Membrane preparations from cells expressing the cDNAs were subjected to high-resolution two-dimensional polyacrylamide gel electrophoresis followed by [alpha-32P]GTP ligand blotting. We have mapped 28 small GTP-binding proteins relative to their isoelectric points and according to their molecular weights and by immunoblotting with specific antibodies. Rab and Rho proteins could be specifically identified by extraction of streptolysin O-permeabilized Madin-Darby canine kidney (MDCK) cells with Rab- and Rho-GDP dissociation inhibitor. We applied the reference mapping to analyze the GTP-binding patterns of synaptosome fractions from rat brain. The purified synaptosomes exhibited specific enrichment of Rab3a, Rab5a, Ral, and several other GTPases. This approach and the map we have produced should provide a useful aid for the analysis of the expression and localization of members of all families of small GTP-binding proteins in various cell types and subcellular fractions.
为了在二维聚丙烯酰胺凝胶上鉴定Rab、Rac、Rho、Ral、Rap和Arf蛋白,我们利用T7 RNA聚合酶-重组痘苗病毒表达系统表达了这些蛋白家族成员的全长cDNA。对表达cDNA的细胞的膜制剂进行高分辨率二维聚丙烯酰胺凝胶电泳,然后进行[α-32P]GTP配体印迹分析。我们根据其等电点、分子量并通过用特异性抗体进行免疫印迹,对28种小GTP结合蛋白进行了定位。Rab和Rho蛋白可以通过用Rab-和Rho-GDP解离抑制剂提取经链球菌溶血素O通透的Madin-Darby犬肾(MDCK)细胞来特异性鉴定。我们应用参考图谱分析大鼠脑突触体组分的GTP结合模式。纯化的突触体显示出Rab3a、Rab5a、Ral和其他几种GTP酶的特异性富集。我们所采用的这种方法和制作的图谱应该为分析各种细胞类型和亚细胞组分中所有小GTP结合蛋白家族成员的表达和定位提供有用的帮助。