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人类免疫缺陷病毒样、非复制性的gag-env颗粒在重组痘苗病毒表达系统中组装。

Human immunodeficiency virus-like, nonreplicating, gag-env particles assemble in a recombinant vaccinia virus expression system.

作者信息

Haffar O, Garrigues J, Travis B, Moran P, Zarling J, Hu S L

机构信息

Department of Virology, Oncogen, Seattle, Washington 98121.

出版信息

J Virol. 1990 Jun;64(6):2653-9. doi: 10.1128/JVI.64.6.2653-2659.1990.

Abstract

We report the assembly of human immunodeficiency virus (HIV)-like particles in African green monkey kidney cells coinfected with two recombinant vaccinia viruses, one carrying the HIV-1 gag and protease genes and the other the env gene. Biochemical analysis of particles sedimented from culture supernatants of doubly infected cells revealed that they were composed of gag proteins, primarily p24, as well as the env proteins gp120 and gp41. Thin-section immunoelectron microscopy showed that these particles were 100 to 120 nm in diameter, were characterized by the presence of cylindrical core structures, and displayed the mature gp120-gp41 complexes on their surfaces. Furthermore, thin-section immunoelectron microscopy analysis of infected cells showed that particle assembly and budding occurred at the plasma membrane. Nucleic acid hybridization suggested that the particles packaged only the gag mRNA but not the env mRNA. Therefore, the system we present is well suited for studies of HIV virion maturation. In addition, the HIV-like particles provide a novel and attractive approach for vaccine development.

摘要

我们报道了在同时感染两种重组痘苗病毒的非洲绿猴肾细胞中组装人免疫缺陷病毒(HIV)样颗粒的情况,其中一种携带HIV-1的gag和蛋白酶基因,另一种携带env基因。对从双重感染细胞的培养上清液中沉淀的颗粒进行生化分析发现,它们由gag蛋白(主要是p24)以及env蛋白gp120和gp41组成。超薄切片免疫电子显微镜显示,这些颗粒直径为100至120纳米,其特征是存在圆柱形核心结构,并且在其表面展示出成熟的gp120-gp41复合物。此外,对感染细胞的超薄切片免疫电子显微镜分析表明,颗粒组装和出芽发生在质膜处。核酸杂交表明,这些颗粒仅包装gag mRNA,而不包装env mRNA。因此,我们所展示的系统非常适合用于研究HIV病毒体的成熟。此外,HIV样颗粒为疫苗开发提供了一种新颖且有吸引力的方法。

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