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禽痘病毒多肽:序列出现及病毒体相关多肽

Fowlpox virus polypeptides: sequential appearance and virion associated polypeptides.

作者信息

Prideaux C T, Boyle D B

机构信息

Department of Microbiology, John Curtin School of Medical Research, Australian National University, Canberra, A.C.T.

出版信息

Arch Virol. 1987;96(3-4):185-99. doi: 10.1007/BF01320959.

Abstract

The polypeptides associated with fowlpox virus (FPV) infection of chicken embryo skin (CES) cells were examined by metabolic labelling with [35S]-methionine and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Polypeptide synthesis was followed over the first 48 hours post infection, as this was shown to be the period of viable virus production in CES cells. In contrast to infection with vaccinia virus (VV), which leads to a rapid total inhibition of host polypeptide synthesis in a number of cell lines, FPV infection of CES cells failed to cause a complete shut down of host polypeptide synthesis, with only a small number of host polypeptides being inhibited. A total of 21 FPV coded or induced polypeptides were resolved by metabolic labelling. As with VV, these polypeptides can be divided into two groups, the pre-replicative polypeptides containing a single member of 70,000 daltons, synthesised before viral DNA replication, and the post-replicative polypeptides, synthesised only after viral DNA replication has commenced. FPV DNA replication was shown to commence between 12 and 16 hours post-infection and to continue up to 48 hours post-infection. As also observed with VV, two temporally distinct classes of post-replicative polypeptides were identified based on their time of synthesis post-infection. The examination of purified FPV and VV by SDS-PAGE and coomassie blue staining allowed the resolution of 57 FPV particle associated polypeptides and 27 VV associated polypeptides.

摘要

通过用[35S]-甲硫氨酸进行代谢标记以及十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE),对与鸡胚皮肤(CES)细胞的禽痘病毒(FPV)感染相关的多肽进行了检测。在感染后的头48小时内跟踪多肽合成情况,因为这被证明是CES细胞中产生有活力病毒的时期。与痘苗病毒(VV)感染不同,痘苗病毒感染会导致许多细胞系中的宿主多肽合成迅速完全受到抑制,而CES细胞的FPV感染并未导致宿主多肽合成完全停止,只有少数宿主多肽受到抑制。通过代谢标记共解析出21种FPV编码或诱导的多肽。与VV一样,这些多肽可分为两组,即复制前期多肽,包含一种70,000道尔顿的单一成分,在病毒DNA复制之前合成;以及复制后期多肽,仅在病毒DNA复制开始后合成。已证明FPV DNA复制在感染后12至16小时开始,并持续至感染后48小时。同样在VV中观察到的情况,根据感染后合成时间,鉴定出了两类在时间上不同的复制后期多肽。通过SDS-PAGE和考马斯亮蓝染色对纯化的FPV和VV进行检测,可分辨出57种与FPV颗粒相关的多肽和27种与VV相关的多肽。

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