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HIV-Gag VLPs presenting trimeric HIV-1 gp140 spikes constitutively expressed in stable double transfected insect cell line

机译:在稳定的双重转染昆虫细胞系中组成性表达三聚体HIV-1 gp140峰的HIV-Gag VLP

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摘要

We have previously described the establishment and characterization of a stably transfected insect cell line for the constitutive and efficient expression of Pr55 HIV Gag proteins, which auto-assemble into enveloped Virus-Like Particles (VLPs) released into the cell culture supernatant. Such HIV-Gag VLPs have been shown to elicit a specific systemic humoral response in vivo, proving the appropriate antigenic presentation of the HIV Gag protein to the immune system. Here we describe the establishment of a stable double transfected insect cell line for the constitutive and reproducible production of Pr55Gag-VLPs expressing on their surface trimeric forms of HIV-1 envelope glycoproteins. The persistence of HIV coding genes has been verified in clonal resistant insect cells, the protein expression and conformation has been verified by Western blot analysis. The resulting HIV-VLPs have been visualized by standard transmission electron microscopy and their immunogenicity has been evaluated in vivo. This represents, to our knowledge, the first example of stable double transfected insect cell line for the constitutive production of enveloped HIV-Gag VLPs presenting trimeric HIV-gp140 on their surface
机译:先前我们已经描述了稳定转染的昆虫细胞系的建立和特性,以用于Pr55 HIV Gag蛋白的组成型和有效表达,该蛋白自动组装成被包膜的病毒样颗粒(VLP),释放到细胞培养上清液中。已经显示出这种HIV-Gag VLP在体内引起特定的体液反应,证明了HIV Gag蛋白向免疫系统的适当抗原呈递。在这里,我们描述了稳定的双转染昆虫细胞系的建立,该细胞系用于在其表面三聚体形式的HIV-1包膜糖蛋白上表达的Pr55Gag-VLP进行组成型和可重复生产。 HIV编码基因的持久性已在抗药性昆虫细胞中得到证实,蛋白质表达和构象已通过蛋白质印迹分析得到证实。所得的HIV-VLPs已通过标准的透射电子显微镜进行了可视化,其免疫原性已在体内进行了评估。据我们所知,这是稳定的双重转染昆虫细胞系的第一个实例,可用于组成型生产在其表面呈三聚体HIV-gp140的包膜HIV-Gag VLP

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