Paterou Athina, Sáez Conde Julia, Týč Jiří, Sunter Jack Daniel, Vaughan Sue, Gull Keith, Dean Samuel
Directorate of Biomedical Sciences, Warwick Medical School, University of Warwick, Coventry, UK.
Department of Biological and Medical Sciences, Oxford Brookes University, Oxford, UK.
Open Biol. 2025 Apr;15(4):240361. doi: 10.1098/rsob.240361. Epub 2025 Apr 2.
African trypanosomes are medically important parasites that cause sleeping sickness in humans and nagana in animals. In addition to their pathogenic role, they have emerged as valuable model organisms for studying fundamental biological processes. Protein tagging is a powerful tool for investigating protein localization and function. In a previous study, we developed two plasmids for rapid and reproducible polymerase chain reaction-based protein tagging in trypanosomes, which enabled the subcellular mapping of 89% of the trypanosome proteome. However, the limited selection of fluorescent protein tags and selectable markers restricted the flexibility of this approach. Here, we present an extended set of >100 plasmids that incorporate universal primer annealing sequences, enabling protein tagging with a range of fluorescent, biochemical and epitope tags, using five different selection markers. We evaluated the suitability of various fluorescent proteins for live and fixed cell imaging, fluorescent movies, and we demonstrate the use of tagging plasmids encoding tandem epitope tags to support expansion microscopy approaches. We show that this series of plasmids is functional in other trypanosomatid parasites, significantly increasing its value. Finally, we developed a new plasmid for tagging glycosylphosphatidylinositol-anchored proteins. We anticipate that this will be an important toolset for investigating trypanosomatid protein localization and function.
非洲锥虫是重要的医学寄生虫,可导致人类昏睡病和动物那加那病。除了其致病作用外,它们已成为研究基本生物学过程的有价值的模式生物。蛋白质标签是研究蛋白质定位和功能的有力工具。在之前的一项研究中,我们开发了两种质粒,用于在锥虫中基于聚合酶链反应进行快速且可重复的蛋白质标签,这使得能够对89%的锥虫蛋白质组进行亚细胞定位。然而,荧光蛋白标签和选择标记的选择有限限制了这种方法的灵活性。在这里,我们展示了一组超过100种的扩展质粒,这些质粒包含通用引物退火序列,能够使用五种不同的选择标记,用一系列荧光、生化和表位标签进行蛋白质标签。我们评估了各种荧光蛋白用于活细胞和固定细胞成像、荧光电影的适用性,并展示了使用编码串联表位标签的标签质粒来支持扩展显微镜方法。我们表明这一系列质粒在其他锥虫寄生虫中也有功能,显著增加了其价值。最后,我们开发了一种用于标记糖基磷脂酰肌醇锚定蛋白的新质粒。我们预计这将成为研究锥虫蛋白质定位和功能的重要工具集。