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痘苗病毒细胞毒素

Vaccinia virus cytotoxin.

作者信息

Wolstenholme J, Woodward C G, Burgoyne R D, Stephen J

出版信息

Arch Virol. 1977;53(1-2):25-37. doi: 10.1007/BF01314844.

Abstract

Extracts of vaccinia-infected HeLa cells were rendered free from infectious virus by centrifugation followed by membrane filtration and were shown to be toxic to uninfected HeLa cells in the presence of hypertonic MgSO4, used as a macromolecular uptake inducer, under conditions which did not kill control cells. Extracts from uninfected cells were nontoxic. This biological test was adapted to a semi-quantitative assay which was used to monitor the purification of the cytotoxic factor by DEAE-cellulose and Sephadex G-100 chromatography. The cytotoxic factor was purified 100-fold, shown to be of molecular weight 30 -- 100,000 daltons, acidic and completely inactivated by soluble trypsin but not by ribonuclease under conditions believed to degrade both single- and double-stranded RNA species. It was demonstrated to be virus specific by approrpiate immunosorbent chromatography. Extracts were also prepared from vaccinia-infected HEp-2, RK and W-K cells respectively. A virus-specific factor, toxic to uninfected HeLa cells, with similar chromatographic properties to that isolated from infected HeLa cells, was isolated from these three additional cell lines. The concept of virus induced cytotoxins, substances which exert their toxic effect in the host cells in which they are made, is discussed.

摘要

将感染痘苗病毒的HeLa细胞提取物通过离心,然后进行膜过滤,使其不含感染性病毒。结果显示,在用作大分子摄取诱导剂的高渗MgSO4存在下,这些提取物对未感染的HeLa细胞有毒性,而在这些条件下对照细胞并未死亡。未感染细胞的提取物则无毒性。这种生物学检测方法被改编为一种半定量测定法,用于监测通过DEAE - 纤维素和葡聚糖凝胶G - 100色谱法对细胞毒性因子的纯化过程。细胞毒性因子被纯化了100倍,其分子量为30 - 100,000道尔顿,呈酸性,在认为能降解单链和双链RNA的条件下,可被可溶性胰蛋白酶完全灭活,但不能被核糖核酸酶灭活。通过适当的免疫吸附色谱法证明其具有病毒特异性。还分别从感染痘苗病毒的HEp - 2、RK和W - K细胞中制备了提取物。从这三种额外的细胞系中分离出了一种对未感染的HeLa细胞有毒性的病毒特异性因子,其色谱特性与从感染的HeLa细胞中分离出的因子相似。文中讨论了病毒诱导细胞毒素的概念,即这些物质在其产生的宿主细胞中发挥毒性作用。

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