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腺病毒相关核酸内切酶的证明

Demonstration of adenovirus associated endonuclease.

作者信息

Medveczky P, Csuzi S, Nász I, Antoni F

出版信息

Acta Microbiol Acad Sci Hung. 1976;23(1):69-76.

PMID:779403
Abstract

In HEp-2 and amnion cell cultures infected with type 1 adenovirus the DNase activity of cell extracts was measured on 32P-labelled Escherichia coli DNA substrate. Enzyme activity was demonstrated by the acid soluble nucleotides released from the 32P-DNA and by the decreased sedimentation rate of labelled DNA. High DNase activity was measured in both adenovirus infected and in untreated HEp-2 cell extracts. Nuclease activity of the amnion host cells being much lower than that of HEp-2 cells, virus-associated endonuclease activity was successfully demonstrated in them. Purified type 1 adenovirus decreased the sedimentation rate of 32P-labelled E. coli DNA. The phenomenon is explained by the virion-associated endonuclease activity. Trypsin inactivated and anti HEp-2 IgG failed to inhibit the virion nuclease. An association between endonuclease and trypsin sensitive penton is assumed.

摘要

在感染1型腺病毒的人喉表皮样癌细胞(HEp - 2)和羊膜细胞培养物中,以32P标记的大肠杆菌DNA为底物,测定细胞提取物的脱氧核糖核酸酶(DNase)活性。通过从32P - DNA释放的酸溶性核苷酸以及标记DNA沉降速率的降低来证明酶活性。在感染腺病毒的和未处理的HEp - 2细胞提取物中均检测到高DNase活性。羊膜宿主细胞的核酸酶活性远低于HEp - 2细胞,因此在其中成功证明了病毒相关的内切核酸酶活性。纯化的1型腺病毒降低了32P标记的大肠杆菌DNA的沉降速率。这种现象可通过病毒体相关的内切核酸酶活性来解释。胰蛋白酶可使其失活,而抗HEp - 2 IgG未能抑制病毒体核酸酶。推测内切核酸酶与对胰蛋白酶敏感的五邻体之间存在关联。

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