Ebola virus VP35 induces high-level production of recombinant TPL-2–ABIN-2–NF-κB1 p105 complex in co-transfected HEK-293 cells

Author:

Gantke Thorsten1,Boussouf Sabrina1,Janzen Julia1,Morrice Nicholas A.2,Howell Steven3,MÜHLBERGER Elke4,Ley Steven C.1

Affiliation:

1. Division of Immune Cell Biology, MRC National Institute for Medical Research, Mill Hill, London NW7 1AA, U.K.

2. Beatson Institute for Cancer Research, Bearsden, Glasgow G61 1BD, U.K.

3. Division of Molecular Structure, MRC National Institute for Medical Research, Mill Hill, London NW7 1AA, U.K.

4. Department of Microbiology, School of Medicine and National Emerging Infectious Disease Laboratories, Boston University, Boston, MA 02118, U.S.A.

Abstract

Activation of PKR (double-stranded-RNA-dependent protein kinase) by DNA plasmids decreases translation, and limits the amount of recombinant protein produced by transiently transfected HEK (human embryonic kidney)-293 cells. Co-expression with Ebola virus VP35 (virus protein 35), which blocked plasmid activation of PKR, substantially increased production of recombinant TPL-2 (tumour progression locus 2)–ABIN-2 [A20-binding inhibitor of NF-κB (nuclear factor κB) 2]–NF-κB1 p105 complex. VP35 also increased expression of other co-transfected proteins, suggesting that VP35 could be employed generally to boost recombinant protein production by HEK-293 cells.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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