Mammalian Cell Display for Antibody Engineering
Open Access
- 10 December 2008
- book chapter
- Published by Springer Nature
- Vol. 525, 337-352
- https://doi.org/10.1007/978-1-59745-554-1_18
Abstract
Antibody engineering has generally been carried out by displaying mouse or human antibodies or antibody fragments on the surface of microorganisms (phage, bacteria, and yeast). We have shown that mammalian cells can be used to display single-chain antibody fragments (scFvs) for affinity maturation. Using mammalian cell display one can isolate and engineer scFvs, Fabs, or whole IgGs for increased affinity and other specific biological functions. Here, we describe a mammalian cell display strategy to isolate high-affinity scFvs specific for CD22. Our strategy uses flow cytometry and human embryonic kidney 293T (HEK-293T) cells that are widely used for transient protein expression. Flow cytometry enhances the screen’s sensitivity thereby allowing us to isolate high-affinity antibodies.Keywords
This publication has 15 references indexed in Scilit:
- Generation and application of a fluorescein-specific single chain antibodyBiochimie, 2007
- Mesothelin targeted cancer immunotherapyEuropean Journal Of Cancer, 2007
- Display technologies: Application for the discovery of drug and gene delivery agents☆Advanced Drug Delivery Reviews, 2006
- Isolation of anti-CD22 Fv with high affinity by Fv display on human cellsProceedings of the National Academy of Sciences, 2006
- Selecting and screening recombinant antibody librariesNature Biotechnology, 2005
- Ligand-assisted Aggregation of ProteinsJournal of Biological Chemistry, 2005
- In Vitro Antibody Evolution Targeting Germline Hot Spots to Increase Activity of an Anti-CD22 ImmunotoxinJournal of Biological Chemistry, 2005
- Selective extraction of polyoma DNA from infected mouse cell culturesPublished by Elsevier ,2004
- Yeast surface display for screening combinatorial polypeptide librariesNature Biotechnology, 1997
- Filamentous Fusion Phage: Novel Expression Vectors That Display Cloned Antigens on the Virion SurfaceScience, 1985