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Yorodumi- EMDB-28939: N332-GT5 SOSIP in complex with V1V3 polyclonal Fabs isolated at d... -
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Basic information
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| Title | N332-GT5 SOSIP in complex with V1V3 polyclonal Fabs isolated at day 42 from mRNA immunized wild type mice | |||||||||
Map data | day 42 V1V3 response main map | |||||||||
Sample |
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Keywords | polyclonal antibodies / mouse antibody / germline targeting / HIV-1 / vaccine design / VIRAL PROTEIN | |||||||||
| Biological species | ![]() ![]() Human immunodeficiency virus | |||||||||
| Method | single particle reconstruction / negative staining / Resolution: 25.0 Å | |||||||||
Authors | Torres JL / Jackson AM / Ozorowski G / Ward AB | |||||||||
| Funding support | United States, 2 items
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Citation | Journal: Science / Year: 2024Title: mRNA-LNP HIV-1 trimer boosters elicit precursors to broad neutralizing antibodies. Authors: Zhenfei Xie / Ying-Cing Lin / Jon M Steichen / Gabriel Ozorowski / Sven Kratochvil / Rashmi Ray / Jonathan L Torres / Alessia Liguori / Oleksandr Kalyuzhniy / Xuesong Wang / John E Warner / ...Authors: Zhenfei Xie / Ying-Cing Lin / Jon M Steichen / Gabriel Ozorowski / Sven Kratochvil / Rashmi Ray / Jonathan L Torres / Alessia Liguori / Oleksandr Kalyuzhniy / Xuesong Wang / John E Warner / Stephanie R Weldon / Gordon A Dale / Kathrin H Kirsch / Usha Nair / Sabyasachi Baboo / Erik Georgeson / Yumiko Adachi / Michael Kubitz / Abigail M Jackson / Sara T Richey / Reid M Volk / Jeong Hyun Lee / Jolene K Diedrich / Thavaleak Prum / Samantha Falcone / Sunny Himansu / Andrea Carfi / John R Yates / James C Paulson / Devin Sok / Andrew B Ward / William R Schief / Facundo D Batista / ![]() Abstract: Germline-targeting (GT) HIV vaccine strategies are predicated on deriving broadly neutralizing antibodies (bnAbs) through multiple boost immunogens. However, as the recruitment of memory B cells ...Germline-targeting (GT) HIV vaccine strategies are predicated on deriving broadly neutralizing antibodies (bnAbs) through multiple boost immunogens. However, as the recruitment of memory B cells (MBCs) to germinal centers (GCs) is inefficient and may be derailed by serum antibody-induced epitope masking, driving further B cell receptor (BCR) modification in GC-experienced B cells after boosting poses a challenge. Using humanized immunoglobulin knockin mice, we found that GT protein trimer immunogen N332-GT5 could prime inferred-germline precursors to the V3-glycan-targeted bnAb BG18 and that B cells primed by N332-GT5 were effectively boosted by either of two novel protein immunogens designed to have minimum cross-reactivity with the off-target V1-binding responses. The delivery of the prime and boost immunogens as messenger RNA lipid nanoparticles (mRNA-LNPs) generated long-lasting GCs, somatic hypermutation, and affinity maturation and may be an effective tool in HIV vaccine development. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_28939.map.gz | 20.6 MB | EMDB map data format | |
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| Header (meta data) | emd-28939-v30.xml emd-28939.xml | 15.5 KB 15.5 KB | Display Display | EMDB header |
| Images | emd_28939.png | 21.7 KB | ||
| Filedesc metadata | emd-28939.cif.gz | 4.5 KB | ||
| Others | emd_28939_half_map_1.map.gz emd_28939_half_map_2.map.gz | 20.6 MB 20.6 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-28939 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-28939 | HTTPS FTP |
-Validation report
| Summary document | emd_28939_validation.pdf.gz | 676.5 KB | Display | EMDB validaton report |
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| Full document | emd_28939_full_validation.pdf.gz | 676 KB | Display | |
| Data in XML | emd_28939_validation.xml.gz | 10.6 KB | Display | |
| Data in CIF | emd_28939_validation.cif.gz | 12.2 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-28939 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-28939 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_28939.map.gz / Format: CCP4 / Size: 27 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | day 42 V1V3 response main map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.77 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: day 42 V1V3 response half map A
| File | emd_28939_half_map_1.map | ||||||||||||
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| Annotation | day 42 V1V3 response half map A | ||||||||||||
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| Density Histograms |
-Half map: day 42 V1V3 response half map B
| File | emd_28939_half_map_2.map | ||||||||||||
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| Annotation | day 42 V1V3 response half map B | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : N332-GT5 SOSIP in complex with V1V3 polyclonal Fabs isolated from...
| Entire | Name: N332-GT5 SOSIP in complex with V1V3 polyclonal Fabs isolated from mRNA immunized wild type mice |
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| Components |
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-Supramolecule #1: N332-GT5 SOSIP in complex with V1V3 polyclonal Fabs isolated from...
| Supramolecule | Name: N332-GT5 SOSIP in complex with V1V3 polyclonal Fabs isolated from mRNA immunized wild type mice type: complex / ID: 1 / Parent: 0 |
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-Supramolecule #2: V1V3 polyclonal Fabs
| Supramolecule | Name: V1V3 polyclonal Fabs / type: complex / ID: 2 / Parent: 1 |
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| Source (natural) | Organism: ![]() |
-Supramolecule #3: N332-GT5 SOSIP
| Supramolecule | Name: N332-GT5 SOSIP / type: complex / ID: 3 / Parent: 1 |
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| Source (natural) | Organism: ![]() Human immunodeficiency virus |
-Experimental details
-Structure determination
| Method | negative staining |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 0.03 mg/mL |
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| Buffer | pH: 7.4 |
| Staining | Type: NEGATIVE / Material: uranyl formate |
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Electron microscopy
| Microscope | FEI TECNAI F20 |
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| Image recording | Film or detector model: TVIPS TEMCAM-F416 (4k x 4k) / Average electron dose: 25.0 e/Å2 |
| Electron beam | Acceleration voltage: 120 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.5 µm / Nominal defocus min: 1.0 µm |
| Experimental equipment | ![]() Model: Tecnai F20 / Image courtesy: FEI Company |
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Image processing
| Startup model | Type of model: PDB ENTRY PDB model - PDB ID: |
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| Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 25.0 Å / Resolution method: FSC 0.5 CUT-OFF / Number images used: 4800 |
| Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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About Yorodumi



Keywords

Human immunodeficiency virus
Authors
United States, 2 items
Citation
















Z (Sec.)
Y (Row.)
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FIELD EMISSION GUN

