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Yorodumi- PDB-7phr: Structure of a fully assembled T-cell receptor engaging a tumor-a... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 7phr | |||||||||||||||||||||||||||
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| Title | Structure of a fully assembled T-cell receptor engaging a tumor-associated peptide-MHC I | |||||||||||||||||||||||||||
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Keywords | IMMUNE SYSTEM / T-cell receptor / TCR / Major Histocompatibility Complex / MHC / Antigen / Adaptive Immunity / Cancer / Complex | |||||||||||||||||||||||||||
| Function / homology | Function and homology informationregulation of lymphocyte apoptotic process / gamma-delta T cell receptor complex / Fc-gamma receptor III complex / cis-Golgi network membrane / positive regulation of melanin biosynthetic process / T cell anergy / positive regulation of cell-cell adhesion mediated by integrin / melanin biosynthetic process / positive regulation of T cell anergy / Fc-gamma receptor signaling pathway ...regulation of lymphocyte apoptotic process / gamma-delta T cell receptor complex / Fc-gamma receptor III complex / cis-Golgi network membrane / positive regulation of melanin biosynthetic process / T cell anergy / positive regulation of cell-cell adhesion mediated by integrin / melanin biosynthetic process / positive regulation of T cell anergy / Fc-gamma receptor signaling pathway / gamma-delta T cell activation / CD4-positive, alpha-beta T cell proliferation / negative thymic T cell selection / melanosome membrane / melanosome organization / multivesicular body, internal vesicle / multivesicular body membrane / positive regulation of CD4-positive, alpha-beta T cell proliferation / alpha-beta T cell receptor complex / positive thymic T cell selection / positive regulation of protein localization to cell surface / signal complex assembly / Nef and signal transduction / positive regulation of memory T cell activation / T cell mediated cytotoxicity directed against tumor cell target / TAP complex binding / Golgi medial cisterna / positive regulation of CD8-positive, alpha-beta T cell activation / CD8-positive, alpha-beta T cell activation / positive regulation of CD8-positive, alpha-beta T cell proliferation / positive regulation of cell-matrix adhesion / smoothened signaling pathway / T cell receptor complex / CD8 receptor binding / Translocation of ZAP-70 to Immunological synapse / Phosphorylation of CD3 and TCR zeta chains / antigen processing and presentation of exogenous peptide antigen via MHC class I / positive regulation of interleukin-4 production / beta-2-microglobulin binding / establishment or maintenance of cell polarity / dendrite development / endoplasmic reticulum exit site / Regulation of MITF-M-dependent genes involved in pigmentation / protein complex oligomerization / TAP binding / antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-dependent / alpha-beta T cell activation / protection from natural killer cell mediated cytotoxicity / Generation of second messenger molecules / FCGR activation / immunological synapse / Co-inhibition by PD-1 / antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent / antigen processing and presentation of endogenous peptide antigen via MHC class Ib / Role of phospholipids in phagocytosis / detection of bacterium / T cell receptor binding / T cell costimulation / positive regulation of T cell proliferation / positive regulation of interleukin-2 production / positive regulation of calcium-mediated signaling / FCGR3A-mediated IL10 synthesis / cell surface receptor protein tyrosine kinase signaling pathway / protein tyrosine kinase binding / negative regulation of receptor binding / T cell activation / early endosome lumen / bioluminescence / Nef mediated downregulation of MHC class I complex cell surface expression / cerebellum development / DAP12 interactions / transferrin transport / cellular response to iron ion / Endosomal/Vacuolar pathway / negative regulation of smoothened signaling pathway / generation of precursor metabolites and energy / lumenal side of endoplasmic reticulum membrane / FCGR3A-mediated phagocytosis / Antigen Presentation: Folding, assembly and peptide loading of class I MHC / peptide antigen assembly with MHC class II protein complex / apoptotic signaling pathway / cellular response to iron(III) ion / MHC class II protein complex / negative regulation of forebrain neuron differentiation / antigen processing and presentation of exogenous protein antigen via MHC class Ib, TAP-dependent / clathrin-coated endocytic vesicle membrane / ER to Golgi transport vesicle membrane / calcium-mediated signaling / peptide antigen assembly with MHC class I protein complex / regulation of iron ion transport / regulation of erythrocyte differentiation / HFE-transferrin receptor complex / response to molecule of bacterial origin / MHC class I peptide loading complex / T cell mediated cytotoxicity / positive regulation of T cell cytokine production / antigen processing and presentation of endogenous peptide antigen via MHC class I / antigen processing and presentation of exogenous peptide antigen via MHC class II / positive regulation of immune response / MHC class I protein complex Similarity search - Function | |||||||||||||||||||||||||||
| Biological species | Homo sapiens (human)![]() | |||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.08 Å | |||||||||||||||||||||||||||
Authors | Susac, L. / Thomas, C. / Tampe, R. | |||||||||||||||||||||||||||
| Funding support | Germany, 4items
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Citation | Journal: Cell / Year: 2022Title: Structure of a fully assembled tumor-specific T cell receptor ligated by pMHC. Authors: Lukas Sušac / Mai T Vuong / Christoph Thomas / Sören von Bülow / Caitlin O'Brien-Ball / Ana Mafalda Santos / Ricardo A Fernandes / Gerhard Hummer / Robert Tampé / Simon J Davis / ![]() Abstract: The T cell receptor (TCR) expressed by T lymphocytes initiates protective immune responses to pathogens and tumors. To explore the structural basis of how TCR signaling is initiated when the ...The T cell receptor (TCR) expressed by T lymphocytes initiates protective immune responses to pathogens and tumors. To explore the structural basis of how TCR signaling is initiated when the receptor binds to peptide-loaded major histocompatibility complex (pMHC) molecules, we used cryogenic electron microscopy to determine the structure of a tumor-reactive TCRαβ/CD3δγεζ complex bound to a melanoma-specific human class I pMHC at 3.08 Å resolution. The antigen-bound complex comprises 11 subunits stabilized by multivalent interactions across three structural layers, with clustered membrane-proximal cystines stabilizing the CD3-εδ and CD3-εγ heterodimers. Extra density sandwiched between transmembrane helices reveals the involvement of sterol lipids in TCR assembly. The geometry of the pMHC/TCR complex suggests that efficient TCR scanning of pMHC requires accurate pre-positioning of T cell and antigen-presenting cell membranes. Comparisons of the ligand-bound and unliganded receptors, along with molecular dynamics simulations, indicate that TCRs can be triggered in the absence of spontaneous structural rearrangements. | |||||||||||||||||||||||||||
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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 | 7phr.cif.gz | 274.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7phr.ent.gz | 214.4 KB | Display | PDB format |
| PDBx/mmJSON format | 7phr.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7phr_validation.pdf.gz | 906.6 KB | Display | wwPDB validaton report |
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| Full document | 7phr_full_validation.pdf.gz | 917.4 KB | Display | |
| Data in XML | 7phr_validation.xml.gz | 49.8 KB | Display | |
| Data in CIF | 7phr_validation.cif.gz | 76.5 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ph/7phr ftp://data.pdbj.org/pub/pdb/validation_reports/ph/7phr | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 13427MC 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
-T-cell receptor ... , 2 types, 2 molecules AB
| #1: Protein | Mass: 27979.268 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: ![]() |
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| #2: Protein | Mass: 32750.736 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: ![]() |
-T-cell surface glycoprotein CD3 ... , 4 types, 6 molecules CDEeZz
| #3: Protein | Mass: 13713.741 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CD3G, T3G / Production host: ![]() | ||
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| #4: Protein | Mass: 39858.188 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human), (gene. exp.) ![]() Gene: CD3D, T3D, GFP / Production host: ![]() | ||
| #5: Protein | Mass: 15316.222 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CD3E, T3E / Production host: ![]() #9: Protein/peptide | Mass: 4138.015 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CD247, CD3Z, T3Z, TCRZ / Production host: ![]() |
-Protein , 2 types, 2 molecules HL
| #6: Protein | Mass: 35054.613 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-A, HLAA / Production host: ![]() |
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| #7: Protein | Mass: 11936.408 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: B2M, CDABP0092, HDCMA22P / Production host: ![]() |
-Protein/peptide / Sugars , 2 types, 7 molecules P

| #10: Sugar | ChemComp-NAG / #8: Protein/peptide | | Mass: 974.107 Da / Num. of mol.: 1 / Mutation: A9V / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human) / References: UniProt: P40967 |
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-Details
| Has ligand of interest | N |
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| Has protein modification | Y |
-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: Fully assembled T-cell receptor engaging a tumor-associated peptide-MHC I Type: COMPLEX / Entity ID: #1-#9 / Source: MULTIPLE SOURCES | ||||||||||||
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| Source (natural) |
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| Source (recombinant) |
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| Buffer solution | pH: 7.5 | ||||||||||||
| 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: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD |
| Image recording | Electron dose: 61 e/Å2 / Film or detector model: GATAN K2 SUMMIT (4k x 4k) |
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Processing
| Software | Name: PHENIX / Version: 1.19.2_4158: / Classification: refinement | ||||||||||||||||||||||||
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| EM software | Name: PHENIX / Category: model refinement | ||||||||||||||||||||||||
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.08 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 154408 / Symmetry type: POINT | ||||||||||||||||||||||||
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About Yorodumi



Homo sapiens (human)

Germany, 4items
Citation

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gel filtration


