Jeansson S, Elwing H, Nygren H, Olofsson S
J Virol Methods. 1982 Apr;4(3):167-76. doi: 10.1016/0166-0934(82)90045-3.
Cell membranes were prepared from herpes simplex virus (HSV) type 1-infected cells and solubilized with a low concentration of sodium deoxycholate. The supernatant after ultracentrifugation was used as antigen in a newly developed solid phase assay, diffusion in gel-enzyme-linked immunosorbent assay (DIG-ELISA). Antigen solubilization was almost complete, all HSV glycoproteins were represented, the yield of antigen in the solubilization process was high, and the presence of a detergent, sodium deoxycholate, did not interfere with the adsorption of antigen to the solid phase. DIG-ELISA was compared with the neutralization test for the determination of HSC antibodies and zone diameters showed a good correlation with the titre obtained by the neutralization test.
从单纯疱疹病毒1型(HSV-1)感染的细胞中制备细胞膜,并用低浓度的脱氧胆酸钠使其溶解。超速离心后的上清液用作新开发的固相检测——凝胶扩散酶联免疫吸附测定(DIG-ELISA)中的抗原。抗原溶解几乎完全,所有HSV糖蛋白均有体现,溶解过程中抗原产量高,并且去污剂脱氧胆酸钠的存在不干扰抗原吸附到固相上。将DIG-ELISA与中和试验进行比较以测定HSV抗体,区域直径与中和试验获得的滴度显示出良好的相关性。