Department of Nephrology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510000, China.
Protein Cell. 2012 Dec;3(12):921-8. doi: 10.1007/s13238-012-2101-y. Epub 2012 Oct 24.
Detection of protein-protein interaction can provide valuable information for investigating the biological function of proteins. The current methods that applied in protein-protein interaction, such as co-immunoprecipitation and pull down etc., often cause plenty of working time due to the burdensome cloning and purification procedures. Here we established a system that characterization of protein-protein interaction was accomplished by co-expression and simply purification of target proteins from one expression cassette within E. coli system. We modified pET vector into co-expression vector pInvivo which encoded PPV NIa protease, two cleavage site F and two multiple cloning sites that flanking cleavage sites. The target proteins (for example: protein A and protein B) were inserted at multiple cloning sites and translated into polyprotein in the order of MBP tag-protein A-site F-PPV NIa protease-site F-protein B-His(6) tag. PPV NIa protease carried out intracellular cleavage along expression, then led to the separation of polyprotein components, therefore, the interaction between protein A-protein B can be detected through one-step purification and analysis. Negative control for protein B was brought into this system for monitoring interaction specificity. We successfully employed this system to prove two cases of reported protien-protein interaction: RHA2a/ANAC and FTA/FTB. In conclusion, a convenient and efficient system has been successfully developed for detecting protein-protein interaction.
蛋白质-蛋白质相互作用的检测可以为研究蛋白质的生物学功能提供有价值的信息。目前应用于蛋白质-蛋白质相互作用的方法,如免疫共沉淀和下拉等,由于克隆和纯化步骤繁琐,往往需要大量的工作时间。在这里,我们建立了一个系统,通过在大肠杆菌系统中一个表达盒中共表达和简单纯化靶蛋白来完成蛋白质-蛋白质相互作用的表征。我们将 pET 载体修改为共表达载体 pInvivo,该载体编码 PPV NIa 蛋白酶、两个切割位点 F 和两个位于切割位点侧翼的多克隆位点。靶蛋白(例如:蛋白 A 和蛋白 B)插入多克隆位点,并以 MBP 标签-蛋白 A-位点 F-PPV NIa 蛋白酶-位点 F-蛋白 B-His(6)标签的顺序翻译为多聚蛋白。PPV NIa 蛋白酶在表达过程中进行细胞内切割,然后导致多聚蛋白成分的分离,因此可以通过一步纯化和分析检测蛋白 A-蛋白 B 之间的相互作用。该系统引入了蛋白 B 的阴性对照用于监测相互作用的特异性。我们成功地利用该系统证明了两种已报道的蛋白-蛋白相互作用的案例:RHA2a/ANAC 和 FTA/FTB。总之,已经成功开发了一种用于检测蛋白质-蛋白质相互作用的方便、高效的系统。