2XKN

Crystal structure of the Fab fragment of the anti-EGFR antibody 7A7

Summary for 2XKN

• Entry DOI: 10.2210/pdb2xkn/pdb
• Descriptor: ANTI-EGFR ANTIBODY 7A7, 2-{2-[2-(2-{2-[2-(2-ETHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL, ... (4 entities in total)
• Functional Keywords: immune system, immunoglobulin
• Biological source: MUS MUSCULUS (HOUSE MOUSE); More
• Total number of polymer chains: 4
• Total formula weight: 96921.93

Authors

Talavera, A.,Mackenzie, J.,Friemann, R.,Krengel, U. (deposition date: 2010-07-09, release date: 2011-06-15, Last modification date: 2024-11-06)

Primary citation

Talavera, A.,Mackenzie, J.,Garrido, G.,Friemann, R.,Lopez-Requena, A.,Moreno, E.,Krengel, U.
Structure of the Fab Fragment of the Anti-Murine Egfr Antibody 7A7 and Exploration of its Receptor Binding Site.
Mol.Immunol., 48:1578-, 2011

PubMed Abstract: The EGF receptor is an important target of cancer immunotherapies. The 7A7 monoclonal antibody has been raised against the murine EGFR, but it cross-reacts with the human receptor. The results from experiments using immune-competent mice can therefore, in principle, be extrapolated to the corresponding scenario in humans. In this work we report the crystal structure of the 7A7 Fab at an effective resolution of 1.4Å. The antibody binding site comprises a deep pocket, located at the interface between the light and heavy chains, with major contributions from CDR loops H1, H2, H3 and L1. Binding experiments show that 7A7 recognizes a site on the EGFR extracellular domain that is not accessible in its most stable conformations, but that becomes exposed upon treatment with a tyrosine kinase inhibitor. This suggests a recognition mechanism similar to that proposed for mAb 806.

PubMed: 21592580
DOI: 10.1016/J.MOLIMM.2011.03.016

Experimental method

X-RAY DIFFRACTION (1.4 Å)