水痘-带状疱疹病毒粒子的纯化及分子解剖。

Biken journal Pub Date : 1983-03-01
C Grose, W E Friedrichs, G C Smith
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引用次数: 0

摘要

收集水痘-带状疱疹病毒(VZV)感染的细胞培养物,并在细胞病变作用进展时进行声破坏。在高盐度(0.5 M)条件下,用8% (w/v)聚乙二醇沉淀,进一步浓缩了超声波中的感染性无细胞病毒,将病毒富集的颗粒层积在15-45%的甲氮酰胺线性梯度上,并在70,000 g下沉积18小时。在三个可见波段(指定为上、中、下)中,在浮力密度为1.156-7 g/cm3的中间波段,包膜病毒粒子富集。电子显微镜下的颗粒计数显示,来自中间带的10.04 log10包膜颗粒和8.26 log10未包膜颗粒代表了150 cm2的vzv感染单层的产量。用SDS-PAGE对放射性标记病毒粒子进行分离,得到30个分子量在30 ~ 200千道尔顿(K)之间的多肽,总摩尔重量为2240,000。主要的结构多肽包括主要的衣壳蛋白(155K)和三个糖蛋白——62K、98K和118K。与[35S]蛋氨酸相比,[14C]氨基酸能更好地标记某些多肽,包括更高摩尔质量的多肽(174K)和与肌动蛋白结合的45K蛋白。nonidet提取的病毒粒子部分的免疫沉淀再次显示了三种主要的糖蛋白,以及155K和45K多肽。将结构多肽与vzv特异性免疫沉淀谱的16种成分进行比较,发现至少有一种多肽(145K)不存在于病毒粒子中,因此被认为是非结构多肽。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Purification and molecular anatomy of the varicella-zoster virion.

Varicella-zoster virus (VZV) infected cell cultures were harvested and sonically disrupted when cytopathic effect was advanced. Infectious cell-free virus in the sonicates, as well as that in the culture medium, was further concentrated by precipitation with 8% (w/v) polyethylene glycol in the presence of high salinity (0.5 M). The virus-enriched pellet was layered onto 15-45% linear metrizamide gradients and sedimented for 18 h at 70,000 g. Of the three visible bands (designated upper, middle and lower), the middle band at a buoyant density of 1.156-7 g/cm3 was enriched for enveloped virions. Electron microscopic enumeration of particles demonstrated a total of 10.04 log10 enveloped particles and 8.26 log10 unenveloped particles from middle bands representing the yield from a 150 cm2 VZV-infected monolayer. Fractionation of radiolabeled virion preparations by SDS-PAGE revealed 30 polypeptides between 30 and 200 kilodaltons (K) with a total mol wt of 2,240,000. Prominent structural polypeptides included the major capsid protein (155K) and three glycoproteins--62K, 98K and 118K. Certain polypeptides better labeled by [14C] amino acids than by [35S] methionine included a higher mol wt polypeptide (174K) and 45K protein comigrating with actin. Immune precipitation of a Nonidet-extracted virion fraction again demonstrated the three major glycoproteins, as well as the 155K and 45K polypeptides. Comparison of structural polypeptides with the 16 constituents of the VZV-specific immunoprecipitation profile identified at least one polypeptide (145K) which was not represented in the virion and assumed, therefore, to be nonstructural.

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