Inducing single-cell suspension of BTI-TN5B1-4 insect cells: I. The use of sulfated polyanions to prevent cell aggregation and enhance recombinant protein production
- 5 May 1997
- journal article
- research article
- Published by Wiley in Biotechnology & Bioengineering
- Vol. 54 (3) , 191-205
- https://doi.org/10.1002/(sici)1097-0290(19970505)54:3<191::aid-bit1>3.0.co;2-a
Abstract
Sulfated polyanions have been successfully used to rapidly obtain and maintain stable single-cell suspension of BTI-TN5B1-4 cells, a cell line which has a high intrinsic capacity for recombinant protein production but clumps severely in suspension reducing its effectiveness as a host for foreign protein production with the baculovirus expression vector system. The efficacy of inducing single-cell suspension correlated positively with the increase in sulfation of the added polyanion. Unsulfated polyanions, neutral polymers, polycations, disaccharides, and monosaccharides were ineffective in inducing single-cell suspension. Elimination of clumping in suspension culture by adding a dispersing agent can lead to enhanced recombinant protein production. Inducing single-cell suspension with dextran sulfate, a highly sulfated polyanion, resulted in a four-fold increase in volumetric yield of the recombinant glycosylated protein, human secreted alkaline phosphatase, and a two-fold increase in volumetric yield of the recombinant cytoplasmic protein, β-galactosidase. High yields of 82 U/ml (ca. 110 mg/L) for alkaline phosphatase, and 705 U/mL (ca. 2.3 g/L) for β-galactosidase under elevated oxygen have been obtained. The optimum volumetric yield of alkaline phosphatase in BTI-TN5B1-4 dextran sulfate cells under elevated oxygen but unsupplemented medium is 6 to 11-fold higher than attached cultures, and 3-fold higher than the best yield obtained for SF21 cells in suspension at elevated oxygen and with nutrient supplementation. More importantly, cells can be infected at high density without complications from aggregation, which has important implications for scale-up. © 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 54:191–205, 1997.Keywords
This publication has 30 references indexed in Scilit:
- Production of Human Alkaline Phosphatase, a Secreted, Glycosylated Protein, from a Baculovirus Expression System and the Attachment‐Dependent Cell Line Trichoplusia ni BTI‐Tn 5B1‐4 Using a Split‐Flow, Air‐Lift BioreactorBiotechnology Progress, 1993
- Optimization of Growth Methods and Recombinant Protein Production in BTI‐Tn‐5B1‐4 Insect Cells Using the Baculovirus Expression SystemBiotechnology Progress, 1993
- Screening of Insect Cell Lines for the Production of Recombinant Proteins and Infectious Virus in the Baculovirus Expression SystemBiotechnology Progress, 1992
- Protein production (?-galactosidase) from a baculovirus vector inSpodoptera frugiperda andTrichpolusia ni cells in suspension cultureBiotechnology Letters, 1991
- Expression of Three Recombinant Proteins Using Baculovirus Vectors in 23 Insect Cell LinesBiotechnology Progress, 1991
- Interaction of dextran sulfate with phospholipid surfaces and liposome aggregation and fusionChemistry and Physics of Lipids, 1990
- Induction of fusion in aggregated and nonaggregated liposomes bearing cationic detergentsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1989
- Human tissue-type plasminogen activator synthesized by using a baculovirus vector in insect cells compared with human plasminogen activator produced in mouse cellsGene, 1988
- Heparin‐induced aggregation of lymphoid cellsJournal of Cellular Physiology, 1986
- Method of colloid titration (a new titration between polymer ions)Journal of Polymer Science, 1952