Suppr超能文献

生产携带 HIV-1 整合酶融合蛋白的慢病毒载体用于基因治疗和蛋白转导。

Production of HIV-1 integrase fusion protein-carrying lentiviral vectors for gene therapy and protein transduction.

机构信息

Department of Biotechnology and Molecular Medicine, A.I. Virtanen Institute for Molecular Sciences, University of Kuopio, FIN-70211 Kuopio, Finland.

出版信息

Hum Gene Ther. 2010 May;21(5):589-602. doi: 10.1089/hum.2009.051.

Abstract

Lentiviral vectors have broad target cell tropism and efficient machinery to integrate transgenes into the host genome. Modification of these vectors by incorporating heterologous proteins into virions has relied mostly on the fusion of proteins into the HIV-1 accessory protein Vpr. Vpr expression can be harmful for cells and its gene has been deleted from third-generation vector production plasmids. We therefore developed a direct integrase fusion protein strategy as an alternative way to package heterologous proteins into vectors. The method was tested by creating two different integrase fusion proteins, IN-p53 and IN-mCherry, cloned into the 3' end of pol in the packaging plasmid. Lentiviral vectors were produced by conventional methods, using the modified packaging plasmids. Vector-incorporated fusion proteins were correctly processed from Gag-Pol, retained the ability to catalyze transgene integration, and showed fusion protein-specific activity by being fluorescent or inducing apoptosis. Functional third-generation lentiviral vectors containing IN-fusion proteins can thus be produced by standard production protocols independent of Vpr expression. Our results suggest that this packaging method is useful for lentiviral vector-mediated protein transduction, such as intranuclear meganuclease, transposon, or zinc finger protein delivery, intracellular imaging of vector particles, and generation of modified lentiviral vectors that contain both toxic and nontoxic IN-fusion proteins.

摘要

慢病毒载体具有广泛的靶细胞嗜性和高效的机制,可将转基因整合到宿主基因组中。通过将异源蛋白融合到病毒粒子中来修饰这些载体,主要依赖于将蛋白质融合到 HIV-1 辅助蛋白 Vpr 中。Vpr 的表达可能对细胞有害,其基因已从第三代载体生产质粒中删除。因此,我们开发了一种直接整合酶融合蛋白策略,作为将异源蛋白包装到载体中的替代方法。该方法通过在包装质粒的 pol 3' 端克隆两种不同的整合酶融合蛋白 IN-p53 和 IN-mCherry 来进行测试。通过常规方法生产慢病毒载体,使用改良的包装质粒。载体中包含的融合蛋白从 Gag-Pol 中正确加工,保留催化转基因整合的能力,并通过荧光或诱导细胞凋亡显示融合蛋白的特异性活性。因此,可以通过标准生产方案生产含有 IN 融合蛋白的功能性第三代慢病毒载体,而无需表达 Vpr。我们的结果表明,这种包装方法可用于慢病毒载体介导的蛋白转导,例如核内核酸酶、转座子或锌指蛋白的递送、载体粒子的细胞内成像以及含有有毒和无毒 IN 融合蛋白的改良慢病毒载体的生成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验