6CHF

Crystal structure of a Fc fragment LALA mutant (L234A, L235A) of human IgG1 (crystal form 1)

Summary for 6CHF

• Entry DOI: 10.2210/pdb6chf/pdb
• Descriptor: Uncharacterized protein DKFZp686C11235, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-[2-acetamido-2-deoxy-beta-D-glucopyranose-(1-2)-alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total)
• Functional Keywords: immunoglobulin, igg1, immune system, immunoglobulin-like beta sandwich, fc fragment, lala mutation
• Biological source: Homo sapiens (Human)
• Total number of polymer chains: 2
• Total formula weight: 51225.28

Authors

Gohain, N.,Tolbert, W.D.,Pazgier, M. (deposition date: 2018-02-22, release date: 2019-02-27, Last modification date: 2024-11-20)

Primary citation

Orlandi, C.,Deredge, D.,Ray, K.,Gohain, N.,Tolbert, W.,DeVico, A.L.,Wintrode, P.,Pazgier, M.,Lewis, G.K.
Antigen-Induced Allosteric Changes in a Human IgG1 Fc Increase Low-Affinity Fc gamma Receptor Binding.
Structure, 2020

PubMed Abstract: Antibody structure couples adaptive and innate immunity via Fab (antigen binding) and Fc (effector) domains that are connected by unique hinge regions. Because antibodies harbor two or more Fab domains, they are capable of crosslinking multi-determinant antigens, which is required for Fc-dependent functions through associative interactions with effector ligands, including C1q and cell surface Fc receptors. The modular nature of antibodies, with distal ligand binding sites for antigen and Fc-ligands, is reminiscent of allosteric proteins, suggesting that allosteric interactions might contribute to Fc-mediated effector functions. This hypothesis has been pursued for over 40 years and remains unresolved. Here, we provide evidence that allosteric interactions between Fab and Fc triggered by antigen binding modulate binding of Fc to low-affinity Fc receptors (FcγR) for a human IgG1. This work opens the path to further dissection of the relative roles of allosteric and associative interactions in Fc-mediated effector functions.

PubMed: 32209433
DOI: 10.1016/j.str.2020.03.001

Experimental method

X-RAY DIFFRACTION (2.4 Å)