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We describe a pipeline for the rapid production of recombinant Fabs derived from mouse monoclonal antibodies suitable for use in structural studies. The pipeline is exemplified by the production of three Fabs derived from the monoclonal antibodies OX108 (anti-CD200 receptor), OX117 and OX119 (anti-SIRPgamma). Heavy and light chain variable domains were inserted into separate expression vectors containing resident constant regions using In-Fusion PCR cloning. Following transient co-expression in HEK 293T cells, secreted Fab fragments were purified by metal chelate chromatography and gel filtration using an automated procedure with yields of up to 4mg/L of cell culture. Following crystallization trials, diffracting crystals were obtained for the recombinant Fabs of OX108 and OX117, and their structures solved to 2.3A and 2.4A, respectively.

Original publication

DOI

10.1016/j.pep.2008.06.017

Type

Journal article

Journal

Protein Expr Purif

Publication Date

11/2008

Volume

62

Pages

83 - 89

Keywords

Amino Acid Sequence, Animals, Antibodies, Monoclonal, Antigens, Surface, Base Sequence, Cells, Cultured, Crystallography, X-Ray, Genetic Vectors, Immunoglobulin Fab Fragments, Mice, Models, Molecular, Molecular Sequence Data, Protein Conformation, Receptors, Cell Surface