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本文引用的文献

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The endoplasmic reticulum as a protein-folding compartment.作为蛋白质折叠区室的内质网。
Trends Cell Biol. 1992 Aug;2(8):227-31. doi: 10.1016/0962-8924(92)90309-b.
2
THE REPLICATION AND COATING OF VACCINIA DNA.痘苗病毒DNA的复制与包膜化
J Mol Biol. 1964 Dec;10:452-74. doi: 10.1016/s0022-2836(64)80066-8.
3
The uptake and development of vaccinia virus in strain L cells followed with labeled viral deoxyribonucleic acid.用标记的病毒脱氧核糖核酸追踪痘苗病毒在L细胞系中的摄取和发育情况。
J Cell Biol. 1963 Jul;18(1):51-72. doi: 10.1083/jcb.18.1.51.
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The initiation of vaccinia infection.牛痘感染的起始
Virology. 1960 Jul;11:603-23. doi: 10.1016/0042-6822(60)90103-3.
5
The vaccinia virus 14-kilodalton fusion protein forms a stable complex with the processed protein encoded by the vaccinia virus A17L gene.痘苗病毒14千道尔顿融合蛋白与痘苗病毒A17L基因编码的加工后蛋白形成稳定复合物。
J Virol. 1993 Jun;67(6):3435-40. doi: 10.1128/JVI.67.6.3435-3440.1993.
6
Assembly of vaccinia virus: role of the intermediate compartment between the endoplasmic reticulum and the Golgi stacks.痘苗病毒的组装:内质网与高尔基体堆栈之间中间区室的作用。
J Cell Biol. 1993 May;121(3):521-41. doi: 10.1083/jcb.121.3.521.
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Folding and assembly of viral membrane proteins.病毒膜蛋白的折叠与组装。
Virology. 1993 Apr;193(2):545-62. doi: 10.1006/viro.1993.1164.
8
Characterization of the budding compartment of mouse hepatitis virus: evidence that transport from the RER to the Golgi complex requires only one vesicular transport step.小鼠肝炎病毒出芽区室的特征:从内质网到高尔基体复合体的转运仅需一个囊泡转运步骤的证据。
J Cell Biol. 1994 Jan;124(1-2):55-70. doi: 10.1083/jcb.124.1.55.
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Assembly of vaccinia virus: effects of rifampin on the intracellular distribution of viral protein p65.痘苗病毒的组装:利福平对病毒蛋白p65细胞内分布的影响
J Virol. 1994 Feb;68(2):1103-14. doi: 10.1128/JVI.68.2.1103-1114.1994.
10
Assembly of vaccinia virus: the second wrapping cisterna is derived from the trans Golgi network.痘苗病毒的组装:第二个包裹池源自反式高尔基体网络。
J Virol. 1994 Jan;68(1):130-47. doi: 10.1128/JVI.68.1.130-147.1994.

痘苗病毒的组装:p14和p32掺入细胞内成熟病毒的膜中。

Assembly of vaccinia virus: incorporation of p14 and p32 into the membrane of the intracellular mature virus.

作者信息

Sodeik B, Cudmore S, Ericsson M, Esteban M, Niles E G, Griffiths G

机构信息

Cell Biology Program, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

J Virol. 1995 Jun;69(6):3560-74. doi: 10.1128/JVI.69.6.3560-3574.1995.

DOI:10.1128/JVI.69.6.3560-3574.1995
PMID:7745704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC189071/
Abstract

The cytoplasmic assembly of vaccinia virus begins with the transformation of a two-membraned cisterna derived from the intermediate compartment between the endoplasmic reticulum and the Golgi complex. This cisterna develops into a viral crescent which eventually forms a spherical immature virus (IV) that matures into the intracellular mature virus (IMV). Using immunoelectron microscopy, we determined the subcellular localization of p32 and p14, two membrane-associated proteins of vaccinia virus. p32 was associated with vaccinia virus membranes at all stages of virion assembly, starting with the viral crescents, as well as with the membranes which accumulated during the inhibition of assembly by rifampin. There was also low but significant labelling of membranes of some cellular compartments, especially those in the vicinity of the Golgi complex. In contrast, anti-p14 labelled neither the crescents nor the IV but gave strong labelling of an intermediate form between IV and IMV and was then associated with all later viral forms. This protein was also not significantly detected on identifiable cellular membranes. Both p32 and p14 were abundantly expressed on the surface of intact IMV. Our data are consistent with a model whereby p32 would become inserted into cellular membranes before being incorporated into the crescents whereas p14 would be posttranslationally associated with the viral outer membrane at a specific later stage of the viral life cycle.

摘要

痘苗病毒的胞质装配始于源自内质网和高尔基体复合体之间中间区室的双膜池的转变。这个池发展成病毒新月体,最终形成球形未成熟病毒(IV),其成熟为细胞内成熟病毒(IMV)。利用免疫电子显微镜,我们确定了痘苗病毒的两种膜相关蛋白p32和p14的亚细胞定位。从病毒新月体开始,p32在病毒体装配的所有阶段都与痘苗病毒膜相关,以及与利福平抑制装配过程中积累的膜相关。一些细胞区室的膜也有低但显著的标记,特别是高尔基体复合体附近的那些膜。相比之下,抗p14既不标记新月体也不标记IV,但对IV和IMV之间的中间形式有强烈标记,然后与所有后续病毒形式相关。在可识别的细胞膜上也未显著检测到这种蛋白。p32和p14在完整IMV的表面都大量表达。我们的数据与一个模型一致,即p32在被纳入新月体之前会插入细胞膜,而p14会在病毒生命周期的特定后期与病毒外膜进行翻译后结合。