Hashimoto K, Simizu B
Arch Virol. 1979;60(3-4):299-309. doi: 10.1007/BF01317501.
Western equine encephalitis virus was disrupted with Triton X-100 and subjected to isoelectric focusing in a sucrose or urea gradient. The two envelope proteins, E1 and E2 were not well separated in a sucrose gradient, while the E1 and E2 proteins were distinguished as two major peaks which focused in a urea gradient at about pH 7.5 and 10, respectively. Isolated E1 protein refocused at pH 6.5 in a sucrose gradient isoelectric focusing column. When Western equine encephalitis virus was treated with Triton X-100 in 0.01 M phosphate buffer (pH6), hemagglutinating E1 protein was solubilized, which isoelectrofocused at pH 6.5. Purified nucleocapsids focused at pH 4 in a sucrose gradient on an isoelectric focusing column. After ribonuclease treatment of the purified nucleocapsid more than 95 per cent of the viral RNA was acid-soluble, and hte nucleocapsid protein isoelectrofocused at about pH 4.
西方马脑炎病毒用Triton X-100处理后,在蔗糖或尿素梯度中进行等电聚焦。在蔗糖梯度中,两种包膜蛋白E1和E2不能很好地分离,而在尿素梯度中,E1和E2蛋白分别聚焦在约pH 7.5和10处,表现为两个主要峰。分离出的E1蛋白在蔗糖梯度等电聚焦柱中于pH 6.5处重新聚焦。当西方马脑炎病毒在0.01 M磷酸盐缓冲液(pH6)中用Triton X-100处理时,具有血凝性的E1蛋白被溶解,其在pH 6.5处等电聚焦。纯化的核衣壳在等电聚焦柱上的蔗糖梯度中于pH 4处聚焦。用核糖核酸酶处理纯化的核衣壳后,超过95%的病毒RNA可酸溶性溶解,核衣壳蛋白在约pH 4处等电聚焦。