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近期关于甲病毒蛋白表达及载体生产的专利。

Recent patents on alphavirus protein expression and vector production.

作者信息

Aranda Alejandro, Ruiz-Guillen Marta, Quetglas Jose I, Bezunartea Jaione, Casales Erkuden, Smerdou Cristian

机构信息

Division of Gene Therapy, School of Medicine, Center for Applied Medical Research, University of Navarra, Av. Pio XII 55, 31008 Pamplona, Spain.

出版信息

Recent Pat Biotechnol. 2011 Dec;5(3):212-26. doi: 10.2174/187220811797579060.

Abstract

Alphaviruses contain a single-strand RNA genome that can be modified to express heterologous genes at high levels. Alphavirus vectors can be packaged within viral particles (VPs) or used as DNA/RNA layered systems. The broad tropism and high expression levels of alphavirus vectors have made them very attractive for applications like recombinant protein expression, vaccination or gene therapy. Expression mediated by alphavirus vectors is generally transient due to induction of apoptosis. However, during the last years several non-cytopathic mutations have been identified within the replicase sequence of different alphaviruses, allowing prolonged protein expression in culture cells. Some of these mutants, which have been patented, have allowed the generation of stable cell lines able to express recombinant proteins for extended periods of time in a constitutive or inducible manner. Production of alphavirus VPs usually requires cotransfection of cells with vector and helper RNAs providing viral structural proteins in trans. During this process full-length wild type (wt) genomes can be generated through recombination between different RNAs. Several new strategies to reduce wt virus generation during packaging, optimize VP production, increase packaging capacity, and provide VPs with specific targeting have been recently patented. Finally, hybrid vectors between alphavirus and other types of viruses have led to a number of patents with applications in vaccination, cancer therapy or retrovirus production.

摘要

甲病毒含有单链RNA基因组,可进行修饰以高水平表达异源基因。甲病毒载体可包装在病毒颗粒(VPs)内或用作DNA/RNA分层系统。甲病毒载体广泛的嗜性和高表达水平使其在重组蛋白表达、疫苗接种或基因治疗等应用中极具吸引力。由于诱导细胞凋亡,甲病毒载体介导的表达通常是瞬时的。然而,在过去几年中,在不同甲病毒的复制酶序列中发现了几种非细胞病变突变,使得在培养细胞中能够延长蛋白表达。其中一些已获专利的突变体能够产生稳定的细胞系,这些细胞系能够以组成型或诱导型方式长时间表达重组蛋白。甲病毒VPs的生产通常需要用载体和辅助RNA共转染细胞,辅助RNA可反式提供病毒结构蛋白。在此过程中,全长野生型(wt)基因组可通过不同RNA之间的重组产生。最近已有多项专利涉及几种新策略,这些策略可减少包装过程中wt病毒的产生、优化VPs生产、增加包装容量以及为VPs提供特异性靶向。最后,甲病毒与其他类型病毒之间的杂交载体已产生了许多专利,可应用于疫苗接种、癌症治疗或逆转录病毒生产。

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