Petre Benjamin, Win Joe, Menke Frank L H, Kamoun Sophien
The Sainsbury Laboratory, Norwich Research Park, Norwich, NR4 7UH, UK.
Methods Mol Biol. 2017;1659:85-98. doi: 10.1007/978-1-4939-7249-4_8.
Plant parasites secrete proteins known as effectors into host tissues to manipulate host cell structures and functions. One of the major goals in effector biology is to determine the host cell compartments and the protein complexes in which effectors accumulate. Here, we describe a five-step pipeline that we routinely use in our lab to achieve this goal, which consists of (1) Golden Gate assembly of pathogen effector-green fluorescent protein (GFP) fusions into binary vectors, (2) Agrobacterium-mediated heterologous protein expression in Nicotiana benthamiana leaf cells, (3) laser-scanning confocal microscopy assay, (4) anti-GFP coimmunoprecipitation-liquid chromatography-tandem mass spectrometry (coIP/MS) assay, and (5) anti-GFP western blotting. This pipeline is suitable for rapid, cost-effective, and medium-throughput screening of pathogen effectors in planta.
植物寄生虫会向宿主组织中分泌被称为效应蛋白的蛋白质,以操控宿主细胞的结构和功能。效应蛋白生物学的主要目标之一是确定效应蛋白在其中积累的宿主细胞区室和蛋白质复合物。在此,我们描述了一种我们实验室常规用于实现这一目标的五步流程,该流程包括:(1)通过金门组装将病原体效应蛋白-绿色荧光蛋白(GFP)融合体构建到二元载体中;(2)农杆菌介导的在本氏烟草叶细胞中的异源蛋白表达;(3)激光扫描共聚焦显微镜检测;(4)抗GFP免疫共沉淀-液相色谱-串联质谱(coIP/MS)检测;以及(5)抗GFP蛋白质免疫印迹法。该流程适用于在植物中对病原体效应蛋白进行快速、经济高效且中等通量的筛选。