Sugita K, Arita H, Sato K, Kawanami J
Biochim Biophys Acta. 1979 Apr 19;552(3):404-12. doi: 10.1016/0005-2736(79)90184-6.
Treatment of Sendai virus with p-(sec-butyl)-phenyl-6-chloro-6-deoxy-beta-D-glucopyranoside, followed by freezing and thawing resulted in a loss of hemolytic and cell fusion activities as well as infectivity without affecting hemagglutinating and neuraminidase activities. The anti-hemolytic activity of this compound was reversed by the addition of phosphatidyl choline to the virus samples. p-Azidophenyl-6-chloro-6-deoxy-beta-D[3H]glucopyranoside was successfully used for photoaffinity labeling of a specific virion site, and we confirmed the affected site of the glucoside to be the lipid components in the viral envelopes.
用对(仲丁基)苯基-6-氯-6-脱氧-β-D-吡喃葡萄糖苷处理仙台病毒,随后进行冻融,导致其溶血和细胞融合活性以及感染性丧失,而血凝和神经氨酸酶活性不受影响。向病毒样品中添加磷脂酰胆碱可逆转该化合物的抗溶血活性。对叠氮基苯基-6-氯-6-脱氧-β-D[3H]吡喃葡萄糖苷成功用于特定病毒粒子位点的光亲和标记,并且我们证实糖苷的作用位点是病毒包膜中的脂质成分。