Shelton L S, Albright A G, Ruyechan W T, Jenkins F J
Department of Microbiology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814.
J Virol. 1994 Jan;68(1):521-5. doi: 10.1128/JVI.68.1.521-525.1994.
The UL37 and ICP8 proteins present in herpes simplex virus type 1 (HSV-1)-infected-cell extracts produced at 24 h postinfection coeluted from single-stranded-DNA-cellulose columns. Experiments carried out with the UL37 protein expressed by a vaccinia virus recombinant (V37) revealed that the UL37 protein did not exhibit DNA-binding activity in the absence of other HSV proteins. Analysis of extracts derived from cells coinfected with V37 and an ICP8-expressing vaccinia virus recombinant (V8) and analysis of extracts prepared from cells infected with the HSV-1 ICP8 deletion mutants d21 and n10 revealed that the retention of the UL37 protein on single-stranded DNA columns required a DNA-binding-competent ICP8 protein.
在感染后24小时产生的单纯疱疹病毒1型(HSV-1)感染细胞提取物中存在的UL37和ICP8蛋白从单链DNA纤维素柱上共同洗脱下来。用痘苗病毒重组体(V37)表达的UL37蛋白进行的实验表明,在没有其他HSV蛋白的情况下,UL37蛋白不表现出DNA结合活性。对与V37和表达ICP8的痘苗病毒重组体(V8)共感染的细胞提取物的分析,以及对感染HSV-1 ICP8缺失突变体d21和n10的细胞制备的提取物的分析表明,UL37蛋白在单链DNA柱上的保留需要具有DNA结合能力的ICP8蛋白。