Significant productivity improvement of the baculovirus expression vector system by engineering a novel expression cassette
Here we describe the development of a baculovirus vector expression cassette containing rearranged baculovirus-derived genetic regulatory elements. This newly designed expression cassette conferred significant production improvements to the baculovirus expression vector system (BEVS), including prol...
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Published in | PloS one Vol. 9; no. 5; p. e96562 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
13.05.2014
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | Here we describe the development of a baculovirus vector expression cassette containing rearranged baculovirus-derived genetic regulatory elements. This newly designed expression cassette conferred significant production improvements to the baculovirus expression vector system (BEVS), including prolonged cell integrity after infection, improved protein integrity, and around 4-fold increase in recombinant protein production yields in insect cells with respect to a standard baculovirus vector. The expression cassette consisted of a cDNA encoding for the baculovirus transactivation factors IE1 and IE0, expressed under the control of the polyhedrin promoter, and a homologous repeated transcription enhancer sequence operatively cis-linked to the p10 promoter or to chimeric promoters containing p10. The prolonged cell integrity observed in cells infected by baculoviruses harbouring the novel expression cassette reduced the characteristic proteolysis and aberrant forms frequently found in baculovirus-derived recombinant proteins. The new expression cassette developed here has the potential to significantly improve the productivity of the BEVS. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: Silvia Gomez-Sebastian and Javier Lopez-Vidal are employees of the company Alternative Gene Expression S.L. (ALGENEX), which exploits and commercializes several patents covering the use of the baculovirus expression cassette described in this work. Jose M. Escribano is one of the founders of ALGENEX and a shareholder of this company. Patents covering the expression cassette described in this manuscript are as follows: PCT/EP2012/061088, Recombinant DNA elements for the expression of recombinant proteins in insects; PCT/EP2012/061081, Recombinant DNA elements for the expression of recombinant proteins in a host cell; PCT/EP2013/075799, Enhanced production of the porcine circovirus capsid protein by a baculovirus vector expression system; and PCT/EP2013/075812, Baculovirus Vector Expression System for the Expression of Recombinant Proteins (in particular virus-like particles). Additionally, we declare that the competing interests declared for all authors do not alter our adherence to PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors. Conceived and designed the experiments: SGS JME. Performed the experiments: SGS JLV. Analyzed the data: SGS JLV JME. Contributed reagents/materials/analysis tools: SGS JLV JME. Wrote the paper: JME. Obtained the financial resources for this work: JME. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0096562 |