Literature DB >> 1369220

Screening of insect cell lines for the production of recombinant proteins and infectious virus in the baculovirus expression system.

T J Wickham1, T Davis, R R Granados, M L Shuler, H A Wood.   

Abstract

Eight cell lines derived from the insects Spodoptera frugiperda, Trichoplusia ni, Mamestra brassicae, and Estigmene acrea were evaluated for recombinant beta-galactosidase and infectious virus production following infection with the baculovirus Autographa californica multiple nuclear polyhedrosis virus (AcMNPV). Production was assessed on a specific (per cell and per microgram of uninfected cellular protein) and on a volumetric (per milliliter) basis. Cell density was found to be an important factor in comparing the cell lines due to a density-dependent inhibition of specific protein and virus production that appeared to result from cell-cell contact. After infection of cells at low-density specific beta-galactosidase production per cell would drop between 3- and 6-fold in five of the eight cell lines when plated on tissue culture plates at near-confluent and confluent cell densities. The cell lines Sf 21 and Sf 9 were least sensitive to cell density. After accounting for cell density effects and differences in cell size, two cell lines, BTI Tn 5B1-4 and BTI TnM, were identified that were superior to the other cell lines, including Sf 21 and Sf 9, in beta-galactosidase production. Optimal volumetric and specific beta-galactosidase production from Tn 5B1-4 and TnM cells was 2-fold and 5-fold higher, respectively, in both cell lines than the optimal production from Sf 9 or Sf 21 cells. The Tn 5B1-4 cell line also had the highest viability of all the cell lines at 3 days postinfection and could be adapted to serum-free media.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1369220     DOI: 10.1021/bp00017a003

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  72 in total

1.  Culture in the rotating-wall vessel affects recombinant protein production capability of two insect cell lines in different manners.

Authors:  M A Saarinen; D W Murhammer
Journal:  In Vitro Cell Dev Biol Anim       Date:  2000-06       Impact factor: 2.416

2.  Stable cell lines expressing baculovirus P35: resistance to apoptosis and nutrient stress, and increased glycoprotein secretion.

Authors:  G Lin; G Li; R R Granados; G W Blissard
Journal:  In Vitro Cell Dev Biol Anim       Date:  2001-05       Impact factor: 2.416

3.  Improved glycosylation of a foreign protein by Tn-5B1-4 cells engineered to express mammalian glycosyltransferases.

Authors:  K Breitbach; D L Jarvis
Journal:  Biotechnol Bioeng       Date:  2001-08-05       Impact factor: 4.530

Review 4.  Developing baculovirus-insect cell expression systems for humanized recombinant glycoprotein production.

Authors:  Donald L Jarvis
Journal:  Virology       Date:  2003-05-25       Impact factor: 3.616

5.  Productivity of insect cells for recombinant proteins.

Authors:  J E Maruniak
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

6.  Insect cell physiology.

Authors:  R Bhatia; G Jesionowski; J Ferrance; M M Ataai
Journal:  Cytotechnology       Date:  1997-05       Impact factor: 2.058

7.  Insect cell physiology.

Authors:  R Bhatia; G Jesionowski; J Ferrance; M M Ataai
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

8.  Insect cell bioreactors.

Authors:  S N Agathos
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

9.  Insect cell cultivation: growth and kinetics.

Authors:  G Schmid
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

10.  Optimization of the production of triabin, a novel thrombin inhibitor, in High Five™ insect cells infected with a recombinant baculovirus.

Authors:  M Vallazza; T Petri
Journal:  Cytotechnology       Date:  1999-03       Impact factor: 2.058

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