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Open data
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Basic information
| Entry | Database: PDB / ID: 7rfp | ||||||
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| Title | Mouse GITR (mGITR) with DTA-1 Fab fragment | ||||||
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Keywords | IMMUNE SYSTEM / Mouse glucocorticoid-induced tumor necrosis factor receptor / mGITR / TNF receptor / DTA-1 | ||||||
| Function / homology | Function and homology informationTNFs bind their physiological receptors / tumor necrosis factor receptor activity / positive regulation of cell adhesion / bioluminescence / generation of precursor metabolites and energy / external side of plasma membrane / apoptotic process / negative regulation of apoptotic process / extracellular region Similarity search - Function | ||||||
| Biological species | ![]() Muromegalovirus G4 | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.4 Å | ||||||
Authors | Meyerson, J.R. / He, C. | ||||||
| Funding support | 1items
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Citation | Journal: Sci Adv / Year: 2022Title: Therapeutic antibody activation of the glucocorticoid-induced TNF receptor by a clustering mechanism. Authors: Changhao He / Rachana R Maniyar / Yahel Avraham / Roberta Zappasodi / Radda Rusinova / Walter Newman / Heidi Heath / Jedd D Wolchok / Rony Dahan / Taha Merghoub / Joel R Meyerson / ![]() Abstract: GITR is a TNF receptor, and its activation promotes immune responses and drives antitumor activity. The receptor is activated by the GITR ligand (GITRL), which is believed to cluster receptors into a ...GITR is a TNF receptor, and its activation promotes immune responses and drives antitumor activity. The receptor is activated by the GITR ligand (GITRL), which is believed to cluster receptors into a high-order array. Immunotherapeutic agonist antibodies also activate the receptor, but their mechanisms are not well characterized. We solved the structure of full-length mouse GITR bound to Fabs from the antibody DTA-1. The receptor is a dimer, and each subunit binds one Fab in an orientation suggesting that the antibody clusters receptors. Binding experiments with purified proteins show that DTA-1 IgG and GITRL both drive extensive clustering of GITR. Functional data reveal that DTA-1 and the anti-human GITR antibody TRX518 activate GITR in their IgG forms but not as Fabs. Thus, the divalent character of the IgG agonists confers an ability to mimic GITRL and cluster and activate GITR. These findings will inform the clinical development of this class of antibodies for immuno-oncology. | ||||||
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Structure visualization
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 7rfp.cif.gz | 181.1 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7rfp.ent.gz | 114.7 KB | Display | PDB format |
| PDBx/mmJSON format | 7rfp.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7rfp_validation.pdf.gz | 822.9 KB | Display | wwPDB validaton report |
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| Full document | 7rfp_full_validation.pdf.gz | 825.9 KB | Display | |
| Data in XML | 7rfp_validation.xml.gz | 36.2 KB | Display | |
| Data in CIF | 7rfp_validation.cif.gz | 59.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/rf/7rfp ftp://data.pdbj.org/pub/pdb/validation_reports/rf/7rfp | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 24444MC M: map data used to model this data C: citing same article ( |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 54848.238 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Muromegalovirus G4Gene: Tnfrsf18, Gitr, eGFP / Production host: Homo sapiens (human) / References: UniProt: O35714, UniProt: A0A7G8ZY66#2: Antibody | Mass: 51014.621 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human)#3: Antibody | Mass: 26320.057 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human)Has protein modification | Y | |
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: mGITR with DTA-1 Fab / Type: COMPLEX / Entity ID: all / Source: MULTIPLE SOURCES |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: Homo sapiens (human) |
| Buffer solution | pH: 8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TALOS ARCTICA |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: OTHER |
| Electron lens | Mode: BRIGHT FIELD |
| Image recording | Electron dose: 55 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 4.4 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 423425 / Symmetry type: POINT |
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Muromegalovirus G4
Citation

UCSF Chimera






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Homo sapiens (human)
