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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-10732 | |||||||||
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| Title | Structure of full-length CD20 in complex with Ofatumumab Fab | |||||||||
Map data | Structure of Human CD20 in complex with Ofatumumab | |||||||||
Sample |
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Keywords | Cancer immunotherapy / Therapeutic antibody / MEMBRANE PROTEIN | |||||||||
| Function / homology | Function and homology informationstore-operated calcium entry / calcium ion import into cytosol / positive regulation of calcium ion import across plasma membrane / epidermal growth factor receptor binding / B cell activation / humoral immune response / B cell proliferation / immunoglobulin binding / plasma membrane raft / B cell differentiation ...store-operated calcium entry / calcium ion import into cytosol / positive regulation of calcium ion import across plasma membrane / epidermal growth factor receptor binding / B cell activation / humoral immune response / B cell proliferation / immunoglobulin binding / plasma membrane raft / B cell differentiation / B cell receptor signaling pathway / response to bacterium / protein tetramerization / MHC class II protein complex binding / cell surface receptor signaling pathway / external side of plasma membrane / cell surface / extracellular space / extracellular exosome / nucleoplasm / identical protein binding / plasma membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.73 Å | |||||||||
Authors | Kumar A / Fronzes R / Reyes N | |||||||||
| Funding support | France, 1 items
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Citation | Journal: Science / Year: 2020Title: Binding mechanisms of therapeutic antibodies to human CD20. Authors: Anand Kumar / Cyril Planchais / Rémi Fronzes / Hugo Mouquet / Nicolas Reyes / ![]() Abstract: Monoclonal antibodies (mAbs) targeting human antigen CD20 (cluster of differentiation 20) constitute important immunotherapies for the treatment of B cell malignancies and autoimmune diseases. Type I ...Monoclonal antibodies (mAbs) targeting human antigen CD20 (cluster of differentiation 20) constitute important immunotherapies for the treatment of B cell malignancies and autoimmune diseases. Type I and II therapeutic mAbs differ in B cell binding properties and cytotoxic effects, reflecting differential interaction mechanisms with CD20. Here we present 3.7- to 4.7-angstrom cryo-electron microscopy structures of full-length CD20 in complexes with prototypical type I rituximab and ofatumumab and type II obinutuzumab. The structures and binding thermodynamics demonstrate that upon binding to CD20, type II mAbs form terminal complexes that preclude recruitment of additional mAbs and complement components, whereas type I complexes act as molecular seeds to increase mAb local concentration for efficient complement activation. Among type I mAbs, ofatumumab complexes display optimal geometry for complement recruitment. The uncovered mechanisms should aid rational design of next-generation immunotherapies targeting CD20. | |||||||||
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Structure visualization
| Movie |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_10732.map.gz | 38.5 MB | EMDB map data format | |
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| Header (meta data) | emd-10732-v30.xml emd-10732.xml | 24.9 KB 24.9 KB | Display Display | EMDB header |
| Images | emd_10732.png | 71.6 KB | ||
| Filedesc metadata | emd-10732.cif.gz | 7 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-10732 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-10732 | HTTPS FTP |
-Validation report
| Summary document | emd_10732_validation.pdf.gz | 516.6 KB | Display | EMDB validaton report |
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| Full document | emd_10732_full_validation.pdf.gz | 515.9 KB | Display | |
| Data in XML | emd_10732_validation.xml.gz | 5.5 KB | Display | |
| Data in CIF | emd_10732_validation.cif.gz | 6.4 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-10732 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-10732 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6y92MC ![]() 6y90C ![]() 6y97C ![]() 6y9aC C: citing same article ( M: atomic model generated by this map |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_10732.map.gz / Format: CCP4 / Size: 75.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Structure of Human CD20 in complex with Ofatumumab | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : Full-length human antigen CD20 in complex with Ofatumumab Fab
| Entire | Name: Full-length human antigen CD20 in complex with Ofatumumab Fab |
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| Components |
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-Supramolecule #1: Full-length human antigen CD20 in complex with Ofatumumab Fab
| Supramolecule | Name: Full-length human antigen CD20 in complex with Ofatumumab Fab type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3 |
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-Supramolecule #2: Full-length human CD20
| Supramolecule | Name: Full-length human CD20 / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #1 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Supramolecule #3: Ofatumumab Fab
| Supramolecule | Name: Ofatumumab Fab / type: complex / ID: 3 / Parent: 1 / Macromolecule list: #2-#3 |
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| Source (natural) | Organism: Homo sapiens (human) / Location in cell: extra cellular |
-Macromolecule #1: B-lymphocyte antigen CD20
| Macromolecule | Name: B-lymphocyte antigen CD20 / type: protein_or_peptide / ID: 1 / Details: Full-length wild type human CD20 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) / Cell: B-lymphocyte |
| Molecular weight | Theoretical: 19.914656 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: TQSFFMRESK TLGAVQIMNG LFHIALGGLL MIPAGIYAPI CVTVWYPLWG GIMYIISGSL LAATEKNSRK CLVKGKMIMN SLSLFAAIS GMILSIMDIL NIKISHFLKM ESLNFIRAHT PYINIYNCEP ANPSEKNSPS TQYCYSIQSL FLGILSVMLI F AFFQELVI AGIVENEWKR UniProtKB: B-lymphocyte antigen CD20 |
-Macromolecule #2: Ofatumumab Fab light chain
| Macromolecule | Name: Ofatumumab Fab light chain / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 23.174719 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: EIVLTQSPAT LSLSPGERAT LSCRASQSVS SYLAWYQQKP GQAPRLLIYD ASNRATGIPA RFSGSGSGTD FTLTISSLEP EDFAVYYCQ QRSNWPITFG QGTRLEIKRT VAAPSVFIFP PSDEQLKSGT ASVVCLLNNF YPREAKVQWK VDNALQSGNS Q ESVTEQDS ...String: EIVLTQSPAT LSLSPGERAT LSCRASQSVS SYLAWYQQKP GQAPRLLIYD ASNRATGIPA RFSGSGSGTD FTLTISSLEP EDFAVYYCQ QRSNWPITFG QGTRLEIKRT VAAPSVFIFP PSDEQLKSGT ASVVCLLNNF YPREAKVQWK VDNALQSGNS Q ESVTEQDS KDSTYSLSST LTLSKADYEK HKVYACEVTH QGLSSPVTKS FNR |
-Macromolecule #3: Ofatumumab Fab heavy chain
| Macromolecule | Name: Ofatumumab Fab heavy chain / type: protein_or_peptide / ID: 3 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 23.138934 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: EVQLVESGGG LVQPGRSLRL SCAASGFTFN DYAMHWVRQA PGKGLEWVST ISWNSGSIGY ADSVKGRFTI SRDNAKKSLY LQMNSLRAE DTALYYCAKD IQYGNYYYGM DVWGQGTTVT VSSASTKGPS VFPLAPGGTA ALGCLVKDYF PEPVTVSWNS G ALTSGVHT ...String: EVQLVESGGG LVQPGRSLRL SCAASGFTFN DYAMHWVRQA PGKGLEWVST ISWNSGSIGY ADSVKGRFTI SRDNAKKSLY LQMNSLRAE DTALYYCAKD IQYGNYYYGM DVWGQGTTVT VSSASTKGPS VFPLAPGGTA ALGCLVKDYF PEPVTVSWNS G ALTSGVHT FPAVLQSSGL YSLSSVVTVP SSSLGTQTYI CNVNHKPSNT KVDKKVEP |
-Macromolecule #4: CHOLESTEROL HEMISUCCINATE
| Macromolecule | Name: CHOLESTEROL HEMISUCCINATE / type: ligand / ID: 4 / Number of copies: 6 / Formula: Y01 |
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| Molecular weight | Theoretical: 486.726 Da |
| Chemical component information | ![]() ChemComp-Y01: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 1.2 mg/mL | |||||||||||||||
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| Buffer | pH: 7.4 Component:
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| Grid | Model: Quantifoil R1.2/1.3 / Material: GOLD / Mesh: 300 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. / Pretreatment - Atmosphere: OTHER | |||||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS GLACIOS |
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| Image recording | Film or detector model: FEI FALCON III (4k x 4k) / Detector mode: COUNTING / Number grids imaged: 1 / Number real images: 2540 / Average exposure time: 40.0 sec. / Average electron dose: 40.0 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 70.0 µm / Calibrated defocus max: 2.2 µm / Calibrated defocus min: 0.8 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm |
| Sample stage | Cooling holder cryogen: NITROGEN |
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Image processing
-Atomic model buiding 1
| Initial model |
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| Refinement | Space: REAL / Protocol: RIGID BODY FIT | ||||||
| Output model | ![]() PDB-6y92: |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
France, 1 items
Citation
UCSF Chimera














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