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Yorodumi- EMDB-27200: SARS-CoV-2 spike protein complexed with polyclonal Fab from donor... -
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Basic information
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| Title | SARS-CoV-2 spike protein complexed with polyclonal Fab from donor A (Donor 1988) | |||||||||
Map data | 3D reconstruction | |||||||||
Sample |
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| Biological species | ![]() Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / negative staining / Resolution: 20.0 Å | |||||||||
Authors | Bangaru S / Sewall LM / Ward AB | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Immunity / Year: 2022Title: Antibodies from primary humoral responses modulate the recruitment of naive B cells during secondary responses. Authors: Jeroen M J Tas / Ja-Hyun Koo / Ying-Cing Lin / Zhenfei Xie / Jon M Steichen / Abigail M Jackson / Blake M Hauser / Xuesong Wang / Christopher A Cottrell / Jonathan L Torres / John E Warner / ...Authors: Jeroen M J Tas / Ja-Hyun Koo / Ying-Cing Lin / Zhenfei Xie / Jon M Steichen / Abigail M Jackson / Blake M Hauser / Xuesong Wang / Christopher A Cottrell / Jonathan L Torres / John E Warner / Kathrin H Kirsch / Stephanie R Weldon / Bettina Groschel / Bartek Nogal / Gabriel Ozorowski / Sandhya Bangaru / Nicole Phelps / Yumiko Adachi / Saman Eskandarzadeh / Michael Kubitz / Dennis R Burton / Daniel Lingwood / Aaron G Schmidt / Usha Nair / Andrew B Ward / William R Schief / Facundo D Batista / ![]() Abstract: Vaccines generate high-affinity antibodies by recruiting antigen-specific B cells to germinal centers (GCs), but the mechanisms governing the recruitment to GCs on secondary challenges remain unclear. ...Vaccines generate high-affinity antibodies by recruiting antigen-specific B cells to germinal centers (GCs), but the mechanisms governing the recruitment to GCs on secondary challenges remain unclear. Here, using preclinical SARS-CoV and HIV mouse models, we demonstrated that the antibodies elicited during primary humoral responses shaped the naive B cell recruitment to GCs during secondary exposures. The antibodies from primary responses could either enhance or, conversely, restrict the GC participation of naive B cells: broad-binding, low-affinity, and low-titer antibodies enhanced recruitment, whereas, by contrast, the high titers of high-affinity, mono-epitope-specific antibodies attenuated cognate naive B cell recruitment. Thus, the directionality and intensity of that effect was determined by antibody concentration, affinity, and epitope specificity. Circulating antibodies can, therefore, be important determinants of antigen immunogenicity. Future vaccines may need to overcome-or could, alternatively, leverage-the effects of circulating primary antibodies on subsequent naive B cell recruitment. | |||||||||
| History |
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_27200.map.gz | 49.1 MB | EMDB map data format | |
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| Header (meta data) | emd-27200-v30.xml emd-27200.xml | 14.5 KB 14.5 KB | Display Display | EMDB header |
| Images | emd_27200.png | 110.9 KB | ||
| Others | emd_27200_half_map_1.map.gz emd_27200_half_map_2.map.gz | 49.4 MB 49.4 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-27200 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-27200 | HTTPS FTP |
-Related structure data
| Related structure data | C: citing same article ( |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_27200.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | 3D reconstruction | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 2.06 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: Half map 2
| File | emd_27200_half_map_1.map | ||||||||||||
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| Annotation | Half map 2 | ||||||||||||
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| Density Histograms |
-Half map: Half map 1
| File | emd_27200_half_map_2.map | ||||||||||||
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| Annotation | Half map 1 | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : SARS-CoV-2 spike protein complexed with polyclonal Fab from donor...
| Entire | Name: SARS-CoV-2 spike protein complexed with polyclonal Fab from donor A (Donor 1988) |
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| Components |
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-Supramolecule #1: SARS-CoV-2 spike protein complexed with polyclonal Fab from donor...
| Supramolecule | Name: SARS-CoV-2 spike protein complexed with polyclonal Fab from donor A (Donor 1988) type: complex / Chimera: Yes / ID: 1 / Parent: 0 |
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-Supramolecule #2: SARS-CoV-2 spike protein
| Supramolecule | Name: SARS-CoV-2 spike protein / type: complex / Chimera: Yes / ID: 2 / Parent: 1 |
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| Source (natural) | Organism: ![]() |
-Supramolecule #3: polyclonal Fab from donor A (Donor 1988)
| Supramolecule | Name: polyclonal Fab from donor A (Donor 1988) / type: complex / Chimera: Yes / ID: 3 / Parent: 1 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Experimental details
-Structure determination
| Method | negative staining |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.4 |
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| Staining | Type: NEGATIVE / Material: uranyl formate |
| Grid | Material: COPPER |
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Electron microscopy
| Microscope | FEI TECNAI SPIRIT |
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| Image recording | Film or detector model: FEI EAGLE (4k x 4k) / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 120 kV / Electron source: LAB6 |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm |
| Experimental equipment | ![]() Model: Tecnai Spirit / Image courtesy: FEI Company |
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Image processing
| Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 20.0 Å / Resolution method: FSC 0.5 CUT-OFF / Number images used: 196462 |
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| Initial angle assignment | Type: OTHER |
| Final angle assignment | Type: OTHER |
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About Yorodumi




Homo sapiens (human)
Authors
United States, 1 items
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