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在基于293的细胞系中组成型游离表达多肽IX(pIX)可弥补5型pIX突变腺病毒的缺陷。

Constitutive episomal expression of polypeptide IX (pIX) in a 293-based cell line complements the deficiency of pIX mutant adenovirus type 5.

作者信息

Caravokyri C, Leppard K N

机构信息

Department of Biological Sciences, Universiy of Warwick, Coventry, United Kingdom.

出版信息

J Virol. 1995 Nov;69(11):6627-33. doi: 10.1128/JVI.69.11.6627-6633.1995.

Abstract

The human adenovirus type 5 capsid is composed of a number of distinct polypeptides. It has been shown previously that one of these, polypeptide IX (pIX), is not absolutely required for the production of viable virus. However, viruses lacking this polypeptide have a significantly reduced packaging limit and, in the one case studied, also show a thermolabile virion phenotype. This report describes the use of eukaryotic episomal vectors based on the Epstein-Barr virus replicon to generate cells which stably express pIX. These cells provide pIX that is efficiently incorporated into virions that are genetically pIX-; such enhanced thermostability. These cells have also been used to isolate a genetically pIX- virus having a genome of length some 2.3 kbp in excess of the previously defined packaging limit for pIX- virus; the resulting virions have wild-type thermostability. These cells expand the theoretical capacity of adenovirus vectors for foreign DNA to around 9.2 kbp and may therefore be useful in gene therapy applications in which vector capacity is limiting.

摘要

人5型腺病毒衣壳由多种不同的多肽组成。先前已经表明,其中一种多肽,即多肽IX(pIX),对于产生有活力的病毒并非绝对必需。然而,缺乏这种多肽的病毒包装极限显著降低,并且在所研究的一个案例中,还表现出热不稳定的病毒粒子表型。本报告描述了使用基于爱泼斯坦 - 巴尔病毒复制子的真核附加型载体来产生稳定表达pIX的细胞。这些细胞提供的pIX能够有效地整合到基因上pIX缺失的病毒粒子中;这种病毒粒子具有增强的热稳定性。这些细胞还被用于分离一种基因上pIX缺失的病毒,其基因组长度比先前定义的pIX缺失病毒的包装极限长约2.3 kbp;产生的病毒粒子具有野生型热稳定性。这些细胞将腺病毒载体对外源DNA的理论容纳能力扩展到约9.2 kbp,因此在载体容量有限的基因治疗应用中可能有用。

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