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人巨细胞病毒被膜蛋白pp150(ppUL32)的核定位

Nuclear localization of the human cytomegalovirus tegument protein pp150 (ppUL32).

作者信息

Hensel G, Meyer H, Gärtner S, Brand G, Kern H F

机构信息

Department of Cell Biology and Cell Pathology, University of Marburg, Germany.

出版信息

J Gen Virol. 1995 Jul;76 ( Pt 7):1591-601. doi: 10.1099/0022-1317-76-7-1591.

Abstract

The human cytomegalovirus (HCMV) basic phosphoprotein pp150, encoded by the UL32 gene, together with the two other major phosphoproteins, pp65 (ppUL83) and pp71 (ppUL82) and several minor structural proteins, form the tegument around the viral nucleocapsid. Experiments were undertaken to locate the area of assembly of tegument proteins pp150 and pp65 and nucleocapsids in fibroblasts, in order to assess the functional role of these two structural proteins in HCMV morphogenesis. Whereas pp150 expression starts during the cytoplasmic maturation of HCMV, pp65 is expressed in the early and late phases of HCMV gene transcription. Western blot analysis of isolated cell fractions showed that pp150 is initially (48 h post-infection) localized in the nucleus, associated either with the nuclear membrane or with viral assembly regions, and later (72 h post-infection) in the cytoplasm. By indirect immunofluorescence, pp150 and pp65 could be detected in nuclear subcompartments and were strongly associated with the nuclear membrane. Using immunogold analysis by electron microscopy, pp65 was exclusively detected within the matrix of cytoplasmic and extracellular dense bodies and of dense body-like structures in the nucleoplasm. These were localized in close contact with hypertrophic nucleoli, in the proximity of developing nucleocapsids and in special patches at the inner nuclear membrane. Positive immunostaining of pp150 was observed at the surface of developing nucleocapsids concentrated within viral assembly regions in the nucleoplasm. Additionally, the tegument of cytoplasmic and extracellular virions was stained, whereas dense bodies or nuclear dense body-like structures did not react. Thus, the acquisition of the tegument protein pp150 seems to start in special nuclear subcompartments of the HCMV-infected fibroblasts.

摘要

人巨细胞病毒(HCMV)的碱性磷蛋白pp150由UL32基因编码,它与另外两种主要的磷蛋白pp65(ppUL83)和pp71(ppUL82)以及几种次要的结构蛋白一起,在病毒核衣壳周围形成包膜。开展实验以确定包膜蛋白pp150和pp65以及核衣壳在成纤维细胞中的组装区域,从而评估这两种结构蛋白在HCMV形态发生中的功能作用。pp150的表达在HCMV的细胞质成熟过程中开始,而pp65在HCMV基因转录的早期和晚期阶段表达。对分离的细胞组分进行的蛋白质免疫印迹分析表明,pp150最初(感染后48小时)定位于细胞核,与核膜或病毒组装区域相关,随后(感染后72小时)定位于细胞质。通过间接免疫荧光法,可在核亚区室中检测到pp150和pp65,它们与核膜紧密相关。利用电子显微镜免疫金分析,仅在细胞质和细胞外致密体以及核质中致密体样结构的基质内检测到pp65。这些致密体样结构与肥大核仁紧密接触,位于正在形成的核衣壳附近以及内核膜的特殊斑块处。在核质中病毒组装区域内聚集的正在形成的核衣壳表面观察到pp150的阳性免疫染色。此外,细胞质和细胞外病毒粒子的包膜被染色,而致密体或核致密体样结构没有反应。因此,包膜蛋白pp150的获得似乎始于HCMV感染的成纤维细胞的特殊核亚区室。

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