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6HGU

Crystal Structure of an anti-APP-tag Fab

Summary for 6HGU
Entry DOI10.2210/pdb6hgu/pdb
Related6HG4 6HG9 6HGA 6HGO
Descriptoranti-APP-tag Fab heavy-chain, anti-APP-tag Fab light-chain, 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, ... (5 entities in total)
Functional Keywordsigg, fab fragment, immune system
Biological sourceMus musculus
More
Total number of polymer chains4
Total formula weight96573.50
Authors
Rondeau, J.M.,Goepfert, A. (deposition date: 2018-08-23, release date: 2019-11-20, Last modification date: 2024-10-23)
Primary citationGoepfert, A.,Lehmann, S.,Blank, J.,Kolbinger, F.,Rondeau, J.M.
Structural Analysis Reveals that the Cytokine IL-17F Forms a Homodimeric Complex with Receptor IL-17RC to Drive IL-17RA-Independent Signaling.
Immunity, 52:499-512.e5, 2020
Cited by
PubMed Abstract: Interleukin-17A (IL-17A), IL-17F, and IL-17A/F heterodimers are key cytokines of the innate and adaptive immune response. Dysregulation of the IL-17 pathway contributes to immune pathology, and it is therefore important to elucidate the molecular mechanisms that govern IL-17 recognition and signaling. The receptor IL-17RC is thought to act in concert with IL-17RA to transduce IL-17A-, IL-17F-, and IL-17A/F-mediated signals. We report the crystal structure of the extracellular domain of human IL-17RC in complex with IL-17F. In contrast to the expected model, we found that IL-17RC formed a symmetrical 2:1 complex with IL-17F, thus competing with IL-17RA for cytokine binding. Using biophysical techniques, we showed that IL-17A and IL-17A/F also form 2:1 complexes with IL-17RC, suggesting the possibility of IL-17RA-independent IL-17 signaling pathways. The crystal structure of the IL-17RC:IL-17F complex provides a structural basis for IL-17F signaling through IL-17RC, with potential therapeutic applications for respiratory allergy and inflammatory bowel diseases.
PubMed: 32187518
DOI: 10.1016/j.immuni.2020.02.004
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

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數據於2024-11-06公開中

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