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5ML9

Cocrystal structure of Fc gamma receptor IIIa interacting with Affimer F4, a specific binding protein which blocks IgG binding to the receptor.

Summary for 5ML9
Entry DOI10.2210/pdb5ml9/pdb
DescriptorLow affinity immunoglobulin gamma Fc region receptor III-A, Affimer F4 with specificity for Fc gamma receptor IIIa, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total)
Functional Keywordsfc gamma receptor iiia affimer competitive inhibitor fcgr3a, immune system
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight34676.97
Authors
Primary citationRobinson, J.I.,Baxter, E.W.,Owen, R.L.,Thomsen, M.,Tomlinson, D.C.,Waterhouse, M.P.,Win, S.J.,Nettleship, J.E.,Tiede, C.,Foster, R.J.,Owens, R.J.,Fishwick, C.W.G.,Harris, S.A.,Goldman, A.,McPherson, M.J.,Morgan, A.W.
Affimer proteins inhibit immune complex binding to Fc gamma RIIIa with high specificity through competitive and allosteric modes of action.
Proc. Natl. Acad. Sci. U.S.A., 115:E72-E81, 2018
Cited by
PubMed Abstract: Protein-protein interactions are essential for the control of cellular functions and are critical for regulation of the immune system. One example is the binding of Fc regions of IgG to the Fc gamma receptors (FcγRs). High sequence identity (98%) between the genes encoding FcγRIIIa (expressed on macrophages and natural killer cells) and FcγRIIIb (expressed on neutrophils) has prevented the development of monospecific agents against these therapeutic targets. We now report the identification of FcγRIIIa-specific artificial binding proteins called "Affimer" that block IgG binding and abrogate FcγRIIIa-mediated downstream effector functions in macrophages, namely TNF release and phagocytosis. Cocrystal structures and molecular dynamics simulations have revealed the structural basis of this specificity for two Affimer proteins: One binds directly to the Fc binding site, whereas the other acts allosterically.
PubMed: 29247053
DOI: 10.1073/pnas.1707856115
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.35 Å)
Structure validation

237735

数据于2025-06-18公开中

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