Delom Frédéric, Fessart Delphine, Caruso Marie-Elaine, Chevet Eric
Department of Surgery, McGill University, Montreal, Que., Canada.
Biochem Biophys Res Commun. 2007 Jan 19;352(3):587-91. doi: 10.1016/j.bbrc.2006.11.046. Epub 2006 Nov 17.
The Tat protein from HIV-1 fused with heterologous proteins traverses biological membranes in a transcellular process called: protein transduction. This has already been successfully exploited in various biological models, but never in the nematode worm Caenorhabditis elegans. TAT-eGFP or GST-eGFP proteins were fed to C. elegans worms, which resulted in the specific localization of Tat-eGFP to epithelial intestinal cells. This system represents an efficient tool for transcellular transduction in C. elegans intestinal cells. Indeed, this approach avoids the use of tedious purification steps to purify the TAT fusion proteins and allows for rapid analyses of the transduced proteins. In addition, it may represent an efficient tool to functionally analyze the mechanisms of protein transduction as well as to complement RNAi/KO in the epithelial intestinal system. To sum up, the advantage of this technology is to combine the potential of bacterial expression system and the Tat-mediated transduction technique in living worm.
来自HIV-1的Tat蛋白与异源蛋白融合后,通过一种称为蛋白转导的跨细胞过程穿过生物膜。这一技术已在各种生物学模型中成功应用,但从未在线虫秀丽隐杆线虫中使用过。将TAT-eGFP或GST-eGFP蛋白喂食给秀丽隐杆线虫,结果Tat-eGFP特异性定位于上皮肠道细胞。该系统是秀丽隐杆线虫肠道细胞跨细胞转导的有效工具。事实上,这种方法避免了使用繁琐的纯化步骤来纯化TAT融合蛋白,并允许对转导蛋白进行快速分析。此外,它可能是一种有效工具,可用于功能分析蛋白转导机制以及补充上皮肠道系统中的RNAi/KO。总之,该技术的优势在于将细菌表达系统的潜力与活线虫中Tat介导的转导技术相结合。