Kohring G W, Mayer F
FEBS Lett. 1987 Jun 1;216(2):207-10. doi: 10.1016/0014-5793(87)80690-7.
Specific IgG antibodies were raised in rabbits against purified EcoRI methylase and restriction endonuclease. Post embedding labeling experiments, using the protein A-gold technique, were made with paraformaldehyde-glutaraldehyde fixed cells, embedded in Lowicryl K4M resin at low temperatures. Labeling with methylase-specific antibodies showed 60-70% of gold particles in the cytoplasm and 30-40% at the cell envelope, whereas the use of restriction enzyme-specific antibodies led to a distribution of 10-30% in the cytoplasm and 70-90% in the cell envelope. The results coincide with the proposed function of the enzymes: in the cytoplasm methylase protects the cells' own DNA from self-destruction, and the restriction endonuclease cuts foreign DNA when entering the cell.
针对纯化的EcoRI甲基化酶和限制性内切酶,在兔体内产生了特异性IgG抗体。采用蛋白A-金技术进行包埋后标记实验,实验对象是用多聚甲醛-戊二醛固定、低温包埋于Lowicryl K4M树脂中的细胞。用甲基化酶特异性抗体标记显示,60%-70%的金颗粒位于细胞质中,30%-40%位于细胞膜;而使用限制性内切酶特异性抗体时,10%-30%的金颗粒分布于细胞质中,70%-90%分布于细胞膜。这些结果与酶的假定功能相符:在细胞质中,甲基化酶保护细胞自身DNA不被自我破坏,而限制性内切酶在外源DNA进入细胞时将其切割。