Usami Makoto, Mitsunaga Katsuyoshi, Nakazawa Ken
Division of Pharmacology, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya, Tokyo 158-8501, Japan.
Toxicol In Vitro. 2007 Apr;21(3):521-6. doi: 10.1016/j.tiv.2006.11.003. Epub 2006 Nov 17.
A simple method for two-dimensional electrophoresis (2-DE) of rat embryonic protein was described. Rat embryos cultured for 24h from day 10.5 of gestation were used as protein samples. Protein samples were lysed in rehydration buffer and separated by isoelectric focusing with immobilized pH gradient for the first dimension and by sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the second dimension. The use of the DeStreak Reagent as an antioxidant in the lysis buffer and electrode pads in the isoelectric focusing greatly improved the 2-DE pattern. When an embryo was used as a protein sample, about 800 protein spots were detected by silver staining in a 2-DE gel of the standard format. Eighty-one protein spots were identified by mass spectrometry for a primary 2-DE map. The same method could be applied to yolk sac membranes from the cultured embryos. The present method was considered to be suitable for a concomitant 2-DE analysis in in vitro developmental toxicity studies.
本文描述了一种用于大鼠胚胎蛋白二维电泳(2-DE)的简单方法。将妊娠第10.5天培养24小时的大鼠胚胎用作蛋白质样品。蛋白质样品在复水缓冲液中裂解,第一维通过固定化pH梯度等电聚焦进行分离,第二维通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行分离。在裂解缓冲液中使用去条纹试剂作为抗氧化剂以及在等电聚焦中使用电极垫极大地改善了二维电泳图谱。当使用胚胎作为蛋白质样品时,在标准格式的二维凝胶中通过银染检测到约800个蛋白质斑点。通过质谱法对初级二维图谱中的81个蛋白质斑点进行了鉴定。相同的方法可应用于培养胚胎的卵黄囊膜。本方法被认为适用于体外发育毒性研究中的二维电泳伴随分析。