Lee Eung-Goo, Kim Jae-Hoon, Shin Yong-Seung, Shin Gee-Wook, Kim Yong-Hwan, Kim Gon-Sup, Kim Dae-Yong, Jung Tae-Sung, Suh Myung-Deuk
Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 600-701, Korea.
J Vet Sci. 2004 Jun;5(2):139-45.
Identification of expressed protein profiles and antigenic determination are some of the most challenging aspects of proteomics. Two-dimensional gel electrophoresis (2-DE) combined with immunoblot analysis were employed to study the N. caninum proteome. Protein sample preparation was carried out by first conducting sonication, followed by adding lysis buffer containing 7M urea plus 2M thiourea to the purified tachyzoites in order to complete disruption. A total of 335 differentially expressed protein spots were detected using pH 4-7 IPG strip (7 cm) that were run in a 56 kVh isoelectric focusing (IEF) system. Of the spots analyzed, 64 were identified as antigenic spots on immunoblot profile. Major antigenic spots appeared at 65 kDa (pI 5.2-5.3), 51 kDa (pI 5.5), 38 kDa (pI 5.1), 33 kDa (pI 4.4), 29 kDa (pI 5.6) and 15.5 kDa (pI 5.0) were observed to be significantly distinct compared to the rest of the antigenic spots. The results indicate that combination of 2-DE and immunoblotting methods were thought as very useful tools in defining both proteins and antigens of N. caninum tachyzoites. Additionally, present 2-DE profiles may be valuable in further proteomic approaches and study of the pathogen.
鉴定表达的蛋白质谱和抗原性测定是蛋白质组学中最具挑战性的一些方面。采用二维凝胶电泳(2-DE)结合免疫印迹分析来研究犬新孢子虫蛋白质组。蛋白质样品制备首先通过超声处理,然后向纯化的速殖子中加入含有7M尿素加2M硫脲的裂解缓冲液以完成细胞破碎。使用在56 kVh等电聚焦(IEF)系统中运行的pH 4-7 IPG条(7 cm)检测到总共335个差异表达的蛋白质斑点。在分析的斑点中,64个在免疫印迹图谱上被鉴定为抗原性斑点。主要抗原性斑点出现在65 kDa(pI 5.2 - 5.3)、51 kDa(pI 5.5)、38 kDa(pI 5.1)、33 kDa(pI 4.4)、29 kDa(pI 5.6)和15.5 kDa(pI 5.0)处,与其余抗原性斑点相比有显著差异。结果表明,2-DE和免疫印迹方法的结合被认为是定义犬新孢子虫速殖子蛋白质和抗原的非常有用的工具。此外,目前的2-DE图谱可能对进一步的蛋白质组学方法和病原体研究有价值。