Zhou Meixian, Fives-Taylor Paula, Wu Hui
Department of Pediatric Dentistry and Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294,USA.
J Microbiol Methods. 2008 Mar;72(3):249-56. doi: 10.1016/j.mimet.2007.12.002. Epub 2007 Dec 15.
There is no systematic examination of affinity tag utility in Gram-positive bacteria, which limits the investigation of protein function in this important group of bacteria as specific antibodies for many of native proteins are generally not available. In this study, we utilized an E. coli-streptococcal shuttle vector pVT1666 and constructed two sets of expression plasmids pVPT-CTag and pVPT-NTag, with each set containing five affinity tags (GST, GFP, HSV, T7 and Nano) that can be fused to either the C- or N-terminus of a target protein. A putative glycosyltransferase (Gtf2) essential for Fap1 glycosylation was used to demonstrate the utility of the cassettes in detection of Gtf2 fusion proteins, and the biological relevance of the proteins in our working strain Streptococcus parasanguinis. GFP and T7 tags were readily expressed in S. parasanguinis as either an N- or C-terminal fusion to Gtf2. Only the C- terminal fusion of GST and HSV were able to be identified in S. parasanguinis. The Nano tag was not detected in either E. coli or S. parasanguinis. Genetic complementation experiments indicated that all the tagged Gtf2 fusion proteins could restore the Gtf2 function in the null mutant except for the Nano-tagged Gtf2 at its N-terminal fusion. Using a T7-tagged Gtf2 fusion construct, we demonstrated that the fusion cassette is also useful in detection of the fusion tag expression in other streptococci including S. mutans, S. pneumoniae and S. sanguinis. Therefore, the expression cassettes we constructed will be a useful tool not only to investigate protein-protein interactions in Fap1 biogenesis in S. parasanguinis, but also to study protein functions in other gram-positive bacteria in which pVT1666 replicates.
目前尚未对革兰氏阳性菌中亲和标签的效用进行系统研究,这限制了对这类重要细菌中蛋白质功能的研究,因为许多天然蛋白质的特异性抗体通常难以获得。在本研究中,我们利用大肠杆菌 - 链球菌穿梭载体pVT1666构建了两组表达质粒pVPT - CTag和pVPT - NTag,每组包含五个亲和标签(GST、GFP、HSV、T7和Nano),这些标签可与目标蛋白质的C端或N端融合。一种对Fap1糖基化至关重要的假定糖基转移酶(Gtf2)被用于证明这些盒式结构在检测Gtf2融合蛋白中的效用,以及这些蛋白质在我们的工作菌株血链球菌中的生物学相关性。GFP和T7标签在血链球菌中能够作为Gtf2的N端或C端融合蛋白轻松表达。在血链球菌中仅能鉴定出GST和HSV的C端融合蛋白。在大肠杆菌或血链球菌中均未检测到Nano标签。基因互补实验表明,除了N端融合的Nano标签化Gtf2外,所有标签化的Gtf2融合蛋白都能在缺失突变体中恢复Gtf2功能。使用T7标签化的Gtf2融合构建体,我们证明了该融合盒式结构在检测包括变形链球菌、肺炎链球菌和血链球菌在内的其他链球菌中的融合标签表达方面也很有用。因此,我们构建的表达盒式结构不仅将成为研究血链球菌中Fap1生物合成中蛋白质 - 蛋白质相互作用的有用工具,还将用于研究pVT1666能够复制的其他革兰氏阳性菌中的蛋白质功能。