Abidi T F, Flanagan T D
J Virol. 1984 May;50(2):380-6. doi: 10.1128/JVI.50.2.380-386.1984.
The glycoproteins HN and F and the lipids were solubilized from Sendai virus envelopes by using the nonionic detergent beta-D-octylglucoside. When beta-D-octylglucoside was removed by dialysis, the glycoproteins and lipids reassociated to form vesicles. These vesicles displayed hemagglutinating, neuraminidase, and hemolysin activities comparable to those expressed by the intact virus. The vesicles were used as carriers to transfer the glycoproteins to the surface of P815 cells. The recipient cells were tested for the acquisition of the glycoproteins by demonstration of surface neuraminidase, hemadsorption activity, and antigens. The modified cells were used as targets for natural cell-mediated lysis and were found to be sensitive.
通过使用非离子去污剂β-D-辛基葡糖苷,从仙台病毒包膜中溶解糖蛋白HN和F以及脂质。通过透析去除β-D-辛基葡糖苷后,糖蛋白和脂质重新结合形成囊泡。这些囊泡表现出与完整病毒所表达的血凝、神经氨酸酶和溶血素活性相当的活性。这些囊泡被用作载体,将糖蛋白转移到P815细胞表面。通过展示表面神经氨酸酶、血细胞吸附活性和抗原,对受体细胞获取糖蛋白的情况进行了检测。修饰后的细胞被用作天然细胞介导裂解的靶标,发现它们是敏感的。