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Yorodumi- EMDB-44893: Cryo-EM structure of rhesus antibody 41328-a.01 in complex with H... -
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Basic information
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| Title | Cryo-EM structure of rhesus antibody 41328-a.01 in complex with HIV-1 Env BG505 DS-SOSIP | |||||||||
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Keywords | Neutralizing antibody / HIV-1 V2 apex / SHIV-elicited / Viral protein / IMMUNE SYSTEM / VIRAL PROTEIN-IMMUNE SYSTEM complex | |||||||||
| Function / homology | Function and homology informationpositive regulation of plasma membrane raft polarization / positive regulation of receptor clustering / host cell endosome membrane / clathrin-dependent endocytosis of virus by host cell / viral protein processing / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / virion attachment to host cell / host cell plasma membrane ...positive regulation of plasma membrane raft polarization / positive regulation of receptor clustering / host cell endosome membrane / clathrin-dependent endocytosis of virus by host cell / viral protein processing / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / virion attachment to host cell / host cell plasma membrane / virion membrane / structural molecule activity / identical protein binding / membrane Similarity search - Function | |||||||||
| Biological species | ![]() ![]() Human immunodeficiency virus 1 | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.96 Å | |||||||||
Authors | Roark RS / Shapiro L / Kwong PD | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: J Exp Med / Year: 2025Title: Structural and genetic basis of HIV-1 envelope V2 apex recognition by rhesus broadly neutralizing antibodies. Authors: Ryan S Roark / Rumi Habib / Jason Gorman / Hui Li / Andrew Jesse Connell / Mattia Bonsignori / Yicheng Guo / Michael P Hogarty / Adam S Olia / Kirsten J Sowers / Baoshan Zhang / Frederic ...Authors: Ryan S Roark / Rumi Habib / Jason Gorman / Hui Li / Andrew Jesse Connell / Mattia Bonsignori / Yicheng Guo / Michael P Hogarty / Adam S Olia / Kirsten J Sowers / Baoshan Zhang / Frederic Bibollet-Ruche / Tatsiana Bylund / Sean Callaghan / John W Carey / Gabriele Cerutti / Darcy R Harris / Wanting He / Emily Lewis / Tracy Liu / Rosemarie D Mason / Yujie Qiao / Younghoon Park / Juliette M Rando / Ajay Singh / Jeremy J Wolff / Q Paula Lei / Mark K Louder / Raiees Andrabi / Nicole A Doria-Rose / Kevin O Saunders / Michael S Seaman / Barton F Haynes / Daniel W Kulp / John R Mascola / Mario Roederer / Theodore C Pierson / Zizhang Sheng / Beatrice H Hahn / George M Shaw / Peter D Kwong / Lawrence Shapiro / ![]() Abstract: Broadly neutralizing antibodies targeting the V2 apex of HIV-1 envelope are desired as vaccine design templates, but few have been described. Here, we report 11 lineages of V2 apex-neutralizing ...Broadly neutralizing antibodies targeting the V2 apex of HIV-1 envelope are desired as vaccine design templates, but few have been described. Here, we report 11 lineages of V2 apex-neutralizing antibodies from simian-human immunodeficiency virus (SHIV)-infected rhesus macaques and determine cryo-EM structures for 9. A single V2 apex-neutralizing lineage accounted for cross-clade breadth in most macaques, and somatic hypermutation relative to breadth was generally low, exemplified by antibody V033-a.01 with <5% nucleotide mutation and 37% breadth (208-strain panel). Envelope complex structures revealed eight different antibody classes (one multi-donor) and the complete repertoire of all five possible recognition topologies, recapitulating canonical human modes of apex insertion and C-strand hydrogen bonding. Despite this diversity in recognition, all rhesus-V2 apex antibodies were derived from reading frame two of the DH3-15*01 gene. Collectively, these results define-in rhesus-the structural and genetic basis of HIV-1 V2 apex recognition and demonstrate unprecedented structural plasticity of a highly selected immunogenetic element. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_44893.map.gz | 108.3 MB | EMDB map data format | |
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| Header (meta data) | emd-44893-v30.xml emd-44893.xml | 23.6 KB 23.6 KB | Display Display | EMDB header |
| Images | emd_44893.png | 136.6 KB | ||
| Filedesc metadata | emd-44893.cif.gz | 7.6 KB | ||
| Others | emd_44893_half_map_1.map.gz emd_44893_half_map_2.map.gz | 200.7 MB 200.2 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-44893 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-44893 | HTTPS FTP |
-Validation report
| Summary document | emd_44893_validation.pdf.gz | 934.6 KB | Display | EMDB validaton report |
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| Full document | emd_44893_full_validation.pdf.gz | 934.2 KB | Display | |
| Data in XML | emd_44893_validation.xml.gz | 15.8 KB | Display | |
| Data in CIF | emd_44893_validation.cif.gz | 18.8 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-44893 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-44893 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9btlMC ![]() 9bnkC ![]() 9bnlC ![]() 9bnmC ![]() 9bnpC ![]() 9bthC ![]() 9btiC ![]() 9btjC ![]() 9btvC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_44893.map.gz / Format: CCP4 / Size: 216 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.83 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #2
| File | emd_44893_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_44893_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Complex of 41328-a.01 with HIV-1 BG505 envelope trimer
| Entire | Name: Complex of 41328-a.01 with HIV-1 BG505 envelope trimer |
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| Components |
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-Supramolecule #1: Complex of 41328-a.01 with HIV-1 BG505 envelope trimer
| Supramolecule | Name: Complex of 41328-a.01 with HIV-1 BG505 envelope trimer type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: Envelope glycoprotein Gp120
| Macromolecule | Name: Envelope glycoprotein Gp120 / type: protein_or_peptide / ID: 1 / Number of copies: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() Human immunodeficiency virus 1 |
| Molecular weight | Theoretical: 53.300348 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: AENLWVTVYY GVPVWKDAET TLFCASDAKA YETEKHNVWA THACVPTDPN PQEIHLENVT EEFNMWKNNM VEQMHTDIIS LWDQSLKPC VKLTPLCVTL QCTNVTNNIT DDMRGELKNC SFNMTTELRD KKQKVYSLFY RLDVVQINEN QGNRSNNSNK E YRLINCNT ...String: AENLWVTVYY GVPVWKDAET TLFCASDAKA YETEKHNVWA THACVPTDPN PQEIHLENVT EEFNMWKNNM VEQMHTDIIS LWDQSLKPC VKLTPLCVTL QCTNVTNNIT DDMRGELKNC SFNMTTELRD KKQKVYSLFY RLDVVQINEN QGNRSNNSNK E YRLINCNT SACTQACPKV SFEPIPIHYC APAGFAILKC KDKKFNGTGP CPSVSTVQCT HGIKPVVSTQ LLLNGSLAEE EV MIRSENI TNNAKNILVQ FNTPVQINCT RPNNNTRKSI RIGPGQAFYA TGDIIGDIRQ AHCNVSKATW NETLGKVVKQ LRK HFGNNT IIRFANSSGG DLEVTTHSFN CGGEFFYCNT SGLFNSTWIS NTSVQGSNST GSNDSITLPC RIKQIINMWQ RIGQ CMYAP PIQGVIRCVS NITGLILTRD GGSTNSTTET FRPGGGDMRD NWRSELYKYK VVKIEPLGVA PTRCKRRVVG R UniProtKB: Envelope glycoprotein gp160 |
-Macromolecule #2: Envelope glycoprotein Gp41
| Macromolecule | Name: Envelope glycoprotein Gp41 / type: protein_or_peptide / ID: 2 / Number of copies: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() Human immunodeficiency virus 1 |
| Molecular weight | Theoretical: 17.075406 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: VGIGAVFLGF LGAAGSTMGA ASMTLTVQAR NLLSGIVQQQ SNLLRAPEAQ QHLLKLTVWG IKQLQARVLA VERYLRDQQL LGIWGCSGK LICCTNVPWN SSWSNRNLSE IWDNMTWLQW DKEISNYTQI IYGLLEESQN QQEKNEQDLL ALD UniProtKB: Envelope glycoprotein gp160 |
-Macromolecule #3: 41328-a.01 heavy chain
| Macromolecule | Name: 41328-a.01 heavy chain / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 26.56757 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: QVQLQQWGEG LVKPSETLSL SCAVYGGSIS GHYYWSWIRQ APGKGLEWIG KIDANSASTN YNPSFKNRVS ISKDTSKKQF YLNLHSVTA ADTAVYYCAR GSIYYEDDDG YYYSEATYLH LHLWGQGVVV TVSSASTKGP SVFPLAPSSR STSESTAALG C LVKDYFPE ...String: QVQLQQWGEG LVKPSETLSL SCAVYGGSIS GHYYWSWIRQ APGKGLEWIG KIDANSASTN YNPSFKNRVS ISKDTSKKQF YLNLHSVTA ADTAVYYCAR GSIYYEDDDG YYYSEATYLH LHLWGQGVVV TVSSASTKGP SVFPLAPSSR STSESTAALG C LVKDYFPE PVTVSWNSGS LTSGVHTFPA VLQSSGLYSL SSVVTVPSSS LGTQTYVCNV NHKPSNTKVD KRVEIKTCGG GL EVLFQ |
-Macromolecule #4: 41328-a.01 light chain
| Macromolecule | Name: 41328-a.01 light chain / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 22.915264 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: QSVLTQPPSA SEAARKRVSI SCSGSFSNIG TNSVSWYQHL PGTAPKLLIY HNGQRASGVS DRFSGSKSGT SASLAISALQ TEDEADYYC ATWDDMLNGY FFGAGTRLTV LGQPKAAPSV TLFPPSSEEL QANKATLVCL ISDFYPGAVE VAWKADGSAV N AGVETTKP ...String: QSVLTQPPSA SEAARKRVSI SCSGSFSNIG TNSVSWYQHL PGTAPKLLIY HNGQRASGVS DRFSGSKSGT SASLAISALQ TEDEADYYC ATWDDMLNGY FFGAGTRLTV LGQPKAAPSV TLFPPSSEEL QANKATLVCL ISDFYPGAVE VAWKADGSAV N AGVETTKP SKQSNNKYAA SSYLSLTSDQ WKSHKSYSCQ VTHEGSTVEK TVAPAECS |
-Macromolecule #10: 2-acetamido-2-deoxy-beta-D-glucopyranose
| Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 10 / Number of copies: 24 / Formula: NAG |
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| Molecular weight | Theoretical: 221.208 Da |
| Chemical component information | ![]() ChemComp-NAG: |
-Experimental details
-Structure determination
| Method | cryo EM |
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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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| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 58.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.8 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords

Human immunodeficiency virus 1
Authors
United States, 1 items
Citation



















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Homo sapiens (human)
Processing
FIELD EMISSION GUN

