Efficient expression of recombinant human monoclonal antibodies in Drosophila S2 cells

• DOI: 10.1016/j.jim.2006.08.017
• Publication Date: 2006-09-26T12:02:52Z
• Authors: Daniel X. Johansson; Katarina Drakenberg; Kathrin H. Hopmann; Alexej Schmidt; Fayezeh Yari; Jorma Hinkula; Mats A.A. Persson
• Keywords: 0301 basic medicine; Blotting, Western; Genetic Vectors; Molecular Sequence Data; Immunoglobulin Variable Region; Antibodies, Monoclonal; Enzyme-Linked Immunosorbent Assay; Transfection; Recombinant Proteins; Cell Line; 3. Good health; 03 medical and health sciences; Microscopy, Fluorescence; Antibody Specificity; Neutralization Tests; Cell Line, Tumor; Immunoglobulin G; HIV-1; Animals; Humans; Drosophila; Immunoglobulin Light Chains; Immunoglobulin Heavy Chains

We have explored the Drosophila S2 cell line for expression of Ig molecules isolated as Fab or scFv cDNA from phage-displayed libraries. We present a series of vectors for inducible expression and secretion of human Ig heavy (HC) and light chains (LC), both on separate plasmids and in combination constructs. Both HC (tested as human gamma(1)) and LC (human kappa) could be expressed separately and were secreted into the medium, confirming previous reports. When the combination vector carrying both the HC and LC cDNA, as well as when the HC and LC vectors were co-transfected, complete IgG1 was found in the medium. Transient transfection resulted in production levels of 0.5-1 mg/l. Stable cell lines could be established within 2-3 weeks. After 10-12 days of expression from such cell lines, Ig molecules accumulated and the medium contained typically 5-35 mg/l of IgG1. The IgG in these preparations was purified to more than 90% purity on protein G columns. Binding characteristics for IgG of the same clone expressed in S2 cells or mammalian cells were indistinguishable. The main advantages with this system compared to mammalian expression were its robustness and the much faster establishment of stable, high level producing cell lines.