Mann E, Edwards J, Brown D T
J Virol. 1983 Mar;45(3):1083-9. doi: 10.1128/JVI.45.3.1083-1089.1983.
The process of cell fusion mediated by Sindbis virus membrane proteins synthesized after infection was examined. At the times after infection at which virus proteins were detectable on the cell surface, Sindbis virus-infected BHK-21 cells were found to express a fusion function after brief treatment at acid pH. In studies employing wild-type virus and temperature-sensitive mutants and testing drug or protease inhibition of virus production, we made the following observations on Sindbis virus-mediated fusion from within. (i) Fusion requires the synthesis of virus glycoproteins and their transport to the cell surface. (ii) Modification of the cell plasma membrane by polypeptides PE2 and E1 alone is not sufficient for expression of the fusion function. (iii) The proteolytic conversion of plasma membrane-associated PE2 to E2 is not essential for fusion. (iv) Glycosylation of virus plasma membrane proteins is essential for fusion. (v) The lesions of Sindbis virus temperature-sensitive mutants do not affect their ability to fuse cells.
对感染后合成的辛德毕斯病毒膜蛋白介导的细胞融合过程进行了研究。在感染后的不同时间,当在细胞表面可检测到病毒蛋白时,发现经酸性pH短暂处理后,感染辛德毕斯病毒的BHK - 21细胞表现出融合功能。在使用野生型病毒和温度敏感突变体以及测试药物或蛋白酶对病毒产生的抑制作用的研究中,我们对辛德毕斯病毒介导的细胞内融合有以下观察结果。(i)融合需要病毒糖蛋白的合成及其运输到细胞表面。(ii)仅由多肽PE2和E1对细胞质膜的修饰不足以表达融合功能。(iii)质膜相关的PE2向E2的蛋白水解转化对于融合不是必需的。(iv)病毒质膜蛋白的糖基化对于融合是必需的。(v)辛德毕斯病毒温度敏感突变体的损伤不影响它们融合细胞的能力。