1QYG

ANTI-COCAINE ANTIBODY M82G2 COMPLEXED WITH BENZOYLECGONINE

Summary for 1QYG

• Entry DOI: 10.2210/pdb1qyg/pdb
• Related: 1Q72
• Descriptor: FAB M82G2, LIGHT CHAIN, FAB M82G2, HEAVY CHAIN, 3-(BENZOYLOXY)-8-METHYL-8-AZABICYCLO[3.2.1]OCTANE-2-CARBOXYLIC ACID, ... (4 entities in total)
• Functional Keywords: anti-cocaine antibody, fab, immune system
• Biological source: Mus musculus (house mouse); More
• Total number of polymer chains: 2
• Total formula weight: 47692.96

Authors

Pozharski, E.,Hewagama, A.,Shanafelt, A.,Petsko, G.,Ringe, D. (deposition date: 2003-09-10, release date: 2003-09-23, Last modification date: 2024-11-06)

Primary citation

Pozharski, E.,Moulin, A.,Hewagama, A.,Shanafelt, A.B.,Petsko, G.A.,Ringe, D.
Diversity in hapten recognition: structural study of an anti-cocaine antibody M82G2.
J.Mol.Biol., 349:570-582, 2005

PubMed Abstract: Antibodies against cocaine and other drugs of abuse are the basis for diagnostic tests for the presence of those drugs in human serum. The 1.7A resolution crystal structure of the anti-cocaine monoclonal antibody M82G2 in complex with cocaine is presented. This structure determination was undertaken to establish the stereochemical features in the antibody binding site that confer specificity for cocaine, and as part of an ongoing project to understand the rules that govern molecular recognition. The cocaine-binding site can be characterized topologically as a narrow groove on the protein surface. The antibody utilizes water-mediated hydrogen bonding, and cation-pi and stacking (pi-pi) interactions to provide specificity. Comparison with the previously published structure of the anti-cocaine antibody GNC92H2 shows that binding of a small ligand can be achieved in diverse ways, both in terms of a binding site structure/topology and protein-ligand interactions.

PubMed: 15885702
DOI: 10.1016/j.jmb.2005.03.080

Experimental method

X-RAY DIFFRACTION (1.81 Å)