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痘病毒K3直系同源物作为构建具有修饰宿主范围的重组痘苗病毒的阳性选择标记的应用。

Application of poxvirus K3 ortholog as a positive selection marker for constructing recombinant vaccinia viruses with modified host range.

作者信息

Cao Jingxin, Layne Christine, Varga Jessie, Deschambault Yvon

机构信息

National Microbiology Laboratory, the Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, Manitoba R3E 3R2, Canada.

Department of Medical Microbiology, University of Manitoba, 543-745 Bannatyne Avenue, Winnipeg, Manitoba R3E 0J9, Canada.

出版信息

MethodsX. 2020 May 15;7:100918. doi: 10.1016/j.mex.2020.100918. eCollection 2020.

Abstract

Vaccinia virus is capable of replicating in a wide range of vertebrate animal cells. However, deletion of the two virus host range genes, E3L and K3L, would render replication of the virus abortive in all the cell types tested, except the cells with defective PKR and RNase L activity. By expressing different poxvirus K3 ortholog proteins in the E3L and K3L double knockout vaccinia virus, we can construct a mutant vaccinia virus with modified host range. Here, using poxvirus K3 ortholog as a positive selection marker, we developed a proof-of-concept protocol to construct recombinant vaccinia viruses expressing foreign proteins. Such a recombinant virus has a modified host range in comparison to wild-type vaccinia virus. This protocol offers the following advantages:➢Cheap: no additional selection reagent is required.➢Highly efficient: nearly all recombinant virus plaques picked would be the stable recombinant virus expressing the protein of interest.➢Rapid: starting from transfection with the recombinant DNA vector, a purified recombinant virus expressing the protein of interest could be obtained within a week.

摘要

痘苗病毒能够在多种脊椎动物细胞中复制。然而,删除两个病毒宿主范围基因E3L和K3L后,除了PKR和RNase L活性有缺陷的细胞外,该病毒在所有测试的细胞类型中复制都会失败。通过在E3L和K3L双敲除痘苗病毒中表达不同的痘病毒K3直系同源蛋白,我们可以构建一种宿主范围经过修饰的突变痘苗病毒。在此,我们以痘病毒K3直系同源蛋白作为阳性选择标记,开发了一种概念验证方案来构建表达外源蛋白的重组痘苗病毒。与野生型痘苗病毒相比,这种重组病毒具有经过修饰的宿主范围。该方案具有以下优点:

➢成本低:无需额外的选择试剂。

➢效率高:几乎所有挑选的重组病毒噬斑都是表达感兴趣蛋白的稳定重组病毒。

➢速度快:从用重组DNA载体转染开始,一周内即可获得表达感兴趣蛋白的纯化重组病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/849d/7264055/0373b21a3904/fx1.jpg

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