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人类和猿猴免疫缺陷病毒的Vif蛋白被包装进病毒粒子,并与病毒核心结构相关联。

The Vif protein of human and simian immunodeficiency viruses is packaged into virions and associates with viral core structures.

作者信息

Liu H, Wu X, Newman M, Shaw G M, Hahn B H, Kappes J C

机构信息

Department of Medicine, University of Alabama at Birmingham 35294, USA.

出版信息

J Virol. 1995 Dec;69(12):7630-8. doi: 10.1128/JVI.69.12.7630-7638.1995.

Abstract

The vif gene of human and simian immunodeficiency viruses (HIV and SIV) encodes a late gene product that is essential for viral infectivity in natural target cells. Virions produced in the absence of Vif are abnormal in their ultrastructural morphology and are severely impaired in the ability to complete proviral DNA synthesis upon entry into new target cells. Because previous studies failed to detect Vif protein in virus particles, Vif is believed to influence virus infectivity indirectly, by affecting virion assembly, release, and/or maturation. In this report, we reexamined the possibility that Vif is a virion-associated protein. Utilizing high-titer Vif-specific antibodies, a sensitive immunoblot technique, and highly concentrated virus preparations, we detected a 23-kDa Vif-reactive protein in wild-type HIV type 1 (HIV-1) and a 27-kDa Vif-reactive protein in wild-type SIVSM virions. Neither protein was present in virions derived from vif-deficient HIV-1 and SIVSM proviral constructs. Vif protein content was similar among different strains of HIV-1 and was independent of the cell type (permissive or nonpermissive) used to produce the virus. To determine the subvirion localization of Vif, HIV-1 virions were treated with proteinase K or Triton X-100 to remove virion surface proteins and the viral membrane, respectively, purified through sucrose, and analyzed by immunoblot analysis. Vif protein content was not affected by the removal of external surface proteins or by the removal of the viral membrane and submembrane p17Gag matrix protein. Instead, Vif colocalized with viral core structures which sedimented at a density of 1.25 g/ml on linear sucrose gradients (enveloped HIV-1 particles sediment at a density of 1.17 g/ml). Finally, the amount of Vif protein packaged into virions was estimated to be on the order of 1 molecule of Vif for every 20 to 30 molecules of p24Gag, or between 60 and 100 molecules of Vif per particle. These results indicate that Vif represents an integral component of HIV and SIV particles and raise the possibility that it plays a direct role in early replication events.

摘要

人类免疫缺陷病毒(HIV)和猿猴免疫缺陷病毒(SIV)的vif基因编码一种晚期基因产物,该产物对于病毒在天然靶细胞中的感染性至关重要。在缺乏Vif的情况下产生的病毒粒子在超微结构形态上异常,并且在进入新靶细胞后完成前病毒DNA合成的能力严重受损。由于先前的研究未能在病毒粒子中检测到Vif蛋白,因此认为Vif通过影响病毒粒子的组装、释放和/或成熟来间接影响病毒感染性。在本报告中,我们重新审视了Vif是一种与病毒粒子相关的蛋白质的可能性。利用高滴度的Vif特异性抗体、灵敏的免疫印迹技术和高浓度的病毒制剂,我们在野生型1型HIV(HIV-1)中检测到一种23 kDa的Vif反应性蛋白,在野生型SIVSM病毒粒子中检测到一种27 kDa的Vif反应性蛋白。在源自vif缺陷型HIV-1和SIVSM前病毒构建体的病毒粒子中均未检测到这两种蛋白。不同HIV-1毒株的Vif蛋白含量相似,并且与用于产生病毒的细胞类型(允许或不允许)无关。为了确定Vif在亚病毒粒子中的定位,用蛋白酶K或Triton X-100分别处理HIV-1病毒粒子以去除病毒粒子表面蛋白和病毒膜,通过蔗糖纯化,并进行免疫印迹分析。去除外部表面蛋白或去除病毒膜和膜下p17Gag基质蛋白均不影响Vif蛋白含量。相反,Vif与病毒核心结构共定位,这些病毒核心结构在线性蔗糖梯度上以1.25 g/ml的密度沉淀(包膜HIV-1颗粒以1.17 g/ml的密度沉淀)。最后,估计包装到病毒粒子中的Vif蛋白量约为每20至30个p24Gag分子中有1个Vif分子,即每个病毒粒子中有60至100个Vif分子。这些结果表明Vif是HIV和SIV粒子的一个组成部分,并增加了它在早期复制事件中起直接作用的可能性。

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