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1型单纯疱疹病毒(HSV-1)衍生的扩增载体。

Herpes simplex virus type 1 (HSV-1)-derived amplicon vectors.

作者信息

Melendez Matias E, Fraefel Cornel, Epstein Alberto L

机构信息

Molecular Oncology Research Center, Barretos Cancer Hospital, 14784-400, Barretos, SP, Brazil.

出版信息

Methods Mol Biol. 2014;1144:81-98. doi: 10.1007/978-1-4939-0428-0_6.

Abstract

Amplicons are defective, helper-dependent, herpes simplex virus type 1 (HSV-1)-derived vectors. The main interest of these vectors as gene transfer tools stems from the fact that the amplicon vector genomes do not carry protein-encoding viral sequences. Consequently, they are completely safe for the host and nontoxic for the infected cells. Moreover, the complete absence of virus genes provides space to accommodate very large foreign DNA sequences, up to almost 150-kb, the size of the virus genome. This large transgene capacity can be used to deliver complete gene loci, including introns and exons, as well as long regulatory sequences, conferring tissue-specific expression or stable maintenance of the transgene in proliferating cells. During many years the development of these vectors and their application in gene transfer experiments was hindered by the presence of contaminating toxic helper virus particles in the vector stocks. In recent years, however, two different methodologies have been developed that allow generating amplicon stocks either completely free of helper particles or only faintly contaminated with fully defective helper particles. This chapter describes these two methodologies.

摘要

扩增子是有缺陷的、依赖辅助病毒的1型单纯疱疹病毒(HSV-1)衍生载体。这些载体作为基因转移工具的主要优势在于,扩增子载体基因组不携带编码蛋白质的病毒序列。因此,它们对宿主完全安全,对感染细胞无毒。此外,完全没有病毒基因提供了容纳非常大的外源DNA序列的空间,几乎可达150 kb,即病毒基因组的大小。这种大的转基因容量可用于传递完整的基因座,包括内含子和外显子,以及长的调控序列,赋予组织特异性表达或使转基因在增殖细胞中稳定维持。多年来,这些载体的开发及其在基因转移实验中的应用因载体储备中存在污染性的有毒辅助病毒颗粒而受到阻碍。然而,近年来,已经开发出两种不同的方法,可生成完全不含辅助颗粒或仅轻微污染有完全缺陷的辅助颗粒的扩增子储备。本章将介绍这两种方法。

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