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Yorodumi- PDB-9jq6: Cryo-EM structure of BTN2A1 in complex with antagonist antibody TH002 -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9jq6 | ||||||
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| Title | Cryo-EM structure of BTN2A1 in complex with antagonist antibody TH002 | ||||||
Components |
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Keywords | IMMUNE SYSTEM / receptor / butyrophilin / antagonist / antibody | ||||||
| Function / homology | Function and homology informationButyrophilin (BTN) family interactions / regulation of cytokine production / lipid metabolic process / T cell receptor signaling pathway / signaling receptor binding / external side of plasma membrane / plasma membrane Similarity search - Function | ||||||
| Biological species | Homo sapiens (human)![]() | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.34 Å | ||||||
Authors | Zhang, M. / Wang, Y.Q. / Xiao, J.Y. | ||||||
| Funding support | China, 1items
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Citation | Journal: Immunity / Year: 2025Title: Structures of butyrophilin multimers reveal a plier-like mechanism for Vγ9Vδ2 T cell receptor activation. Authors: Mai Zhang / Yiqing Wang / Ningning Cai / Yingying Qu / Xianqiang Ma / Jing Xue / Xiaorui Chen / Xueguang Zhang / Junyu Xiao / Yonghui Zhang / ![]() Abstract: Vγ9Vδ2 T cells, the major circulating human γδ T cell subset, respond to infections and tumors by recognizing phosphoantigens (pAgs) via transmembrane butyrophilins (BTN3A1, BTN3A2, and BTN2A1). ...Vγ9Vδ2 T cells, the major circulating human γδ T cell subset, respond to infections and tumors by recognizing phosphoantigens (pAgs) via transmembrane butyrophilins (BTN3A1, BTN3A2, and BTN2A1). Here, using cryoelectron microscopy, we resolved the structures of BTN multimers bound to the microbial pAg HMBPP alone and in complex with the T cell receptor (TCR). These structures reveal that BTN3A1 and BTN2A1 cooperate to sense pAgs through their intracellular B30.2 domains, whereas BTN3A2 and BTN2A1 interact extracellularly. TCR engagement triggers its conformational changes, allowing BTN2A1 to bind the Vγ9 chain laterally and BTN3A2 to interact apically with the Vδ2 chain's germline-encoded regions and CDR3 motif, as well as the Vγ9 CDR3. Our study uncovers a "plier-like gripping" mechanism, where BTN multimers bridge the TCR surface to drive activation. These findings establish a structural foundation for γδ T cell-targeted immunotherapies distinct from αβ T cell strategies reliant on major-histocompatibility-complex-mediated antigen presentation. | ||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9jq6.cif.gz | 273.3 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9jq6.ent.gz | 214.3 KB | Display | PDB format |
| PDBx/mmJSON format | 9jq6.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9jq6_validation.pdf.gz | 603.7 KB | Display | wwPDB validaton report |
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| Full document | 9jq6_full_validation.pdf.gz | 625.7 KB | Display | |
| Data in XML | 9jq6_validation.xml.gz | 29.3 KB | Display | |
| Data in CIF | 9jq6_validation.cif.gz | 44.8 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/jq/9jq6 ftp://data.pdbj.org/pub/pdb/validation_reports/jq/9jq6 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 61724MC ![]() 9jqpC ![]() 9jqqC ![]() 9jqrC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 60015.312 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: BTN2A1, BT2.1, BTF1 / Cell line (production host): HEK293F / Production host: Homo sapiens (human) / References: UniProt: Q7KYR7#2: Antibody | Mass: 24961.285 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() #3: Antibody | Mass: 23813.033 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() #4: Polysaccharide | Source method: isolated from a genetically manipulated source #5: Sugar | ChemComp-NAG / Has ligand of interest | N | 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: full-length BTN2A1 in complex with its antagonist antibody TH002 Type: COMPLEX / Entity ID: #1-#3 / Source: RECOMBINANT | ||||||||||||
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| Molecular weight | Experimental value: NO | ||||||||||||
| Source (natural) |
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| Source (recombinant) | Organism: Homo sapiens (human) / Cell: HEK293F / Plasmid: pcDNA3.1 | ||||||||||||
| Buffer solution | pH: 7.4 | ||||||||||||
| 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: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: TFS KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1700 nm / Nominal defocus min: 1300 nm |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) |
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Processing
| EM software | Name: PHENIX / Version: 1.20.1_4487: / Category: model refinement |
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
| 3D reconstruction | Resolution: 3.34 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 247369 / Symmetry type: POINT |
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About Yorodumi



Homo sapiens (human)

China, 1items
Citation












PDBj



gel filtration

