Rubio N, Cuesta A
Instituto Cajal, Madrid, Spain.
J Virol. 1988 Nov;62(11):4303-6. doi: 10.1128/JVI.62.11.4303-4306.1988.
An immunological assay was developed to characterize the binding of Theiler's murine encephalomyelitis virus to BHK-21 cell receptors. After absorption of the virus and formaldehyde fixation, rabbit antibodies and Staphylococcus aureus protein A labeled with 125I formed a specific complex on the surfaces of the cells. The optimal multiplicity of infection in this system was 10 PFU per cell. The virus was internalized at 33 and 37 degrees C, but internalization did not take place at 25 or 4 degrees C. The binding was proportional to the number of cells and was significant within 30 s. Cell surface receptors were still active after fixation, and only intact viruses were bound, as demonstrated by the lack of binding of the purified, isolated virion proteins VP1, VP2, and VP3.
开发了一种免疫测定法来表征泰勒氏小鼠脑脊髓炎病毒与BHK - 21细胞受体的结合。在病毒吸附和甲醛固定后,兔抗体和用125I标记的金黄色葡萄球菌蛋白A在细胞表面形成特异性复合物。该系统中最佳感染复数为每细胞10个空斑形成单位(PFU)。病毒在33℃和37℃时内化,但在25℃或4℃时不发生内化。结合与细胞数量成正比,且在30秒内显著。固定后细胞表面受体仍有活性,且只有完整病毒能结合,这通过纯化的、分离的病毒粒子蛋白VP1、VP2和VP3缺乏结合得以证明。