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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | Q10M-055 Fab in complex with HIV-1 Env Q23 NFL TD CC3+ | |||||||||
Map data | sharpened map | |||||||||
Sample |
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Keywords | HIV-1 / macaque / non-human primate / NHP / V2-apex / neutralizing antibody / VIRAL PROTEIN-IMMUNE SYSTEM complex | |||||||||
| Biological species | ![]() Human immunodeficiency virus 1 / ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.5 Å | |||||||||
Authors | Phulera S / Ozorowski G / Ward AB | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Nature / Year: 2026Title: Vaccination generates broadly cross-neutralizing antibodies to the HIV Env apex. Authors: Javier Guenaga / Monika Ádori / Shridhar Bale / Swastik Phulera / Ioannis Zygouras / Fabian-Alexander Schleich / Xaquin Castro Dopico / Sashank Agrawal / Miyo Ota / Richard Wilson / Jocelyn ...Authors: Javier Guenaga / Monika Ádori / Shridhar Bale / Swastik Phulera / Ioannis Zygouras / Fabian-Alexander Schleich / Xaquin Castro Dopico / Sashank Agrawal / Miyo Ota / Richard Wilson / Jocelyn Cluff / Tamar Dzvelaia / Marco Mandolesi / Wen-Hsin Lee / Agnes A Walsh / Mariane B Melo / Laurent Verkoczy / Darrell J Irvine / Martin Corcoran / Ian A Wilson / Diane Carnathan / Guido Silvestri / Andrew B Ward / Gabriel Ozorowski / Gunilla B Karlsson Hedestam / Richard T Wyatt / ![]() Abstract: As a chronically replicating virus, HIV has evolved extreme sequence variability and effective shielding of functionally constrained spike protein determinants by host-derived glycans. Broadly ...As a chronically replicating virus, HIV has evolved extreme sequence variability and effective shielding of functionally constrained spike protein determinants by host-derived glycans. Broadly neutralizing antibodies, although rare, can be isolated from people living with HIV, revealing conserved envelope glycoprotein (Env) sites as key targets for vaccine development. One such target is the apex of the Env spike. Here we identify a vaccination strategy using heterologous HIV Env trimers covalently coupled to liposomes for multivalent display that resulted in the elicitation of cross-neutralizing HIV serum antibody responses in all trimer-liposome-immunized non-human primates. Critically, we isolated monoclonal antibodies from multiple macaques that cross-neutralize divergent HIV clinical isolates. High-resolution cryogenic electron microscopy structural analyses of monoclonal antibodies from four different macaques demonstrate that they target the Env trimer apex in a manner highly similar to that of the human-infection-elicited, apex-directed broadly neutralizing antibody PG9, representing a substantial advance in HIV vaccine development. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_72009.map.gz | 230.1 MB | EMDB map data format | |
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| Header (meta data) | emd-72009-v30.xml emd-72009.xml | 21.6 KB 21.6 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_72009_fsc.xml | 13.2 KB | Display | FSC data file |
| Images | emd_72009.png | 110.7 KB | ||
| Masks | emd_72009_msk_1.map | 244.1 MB | Mask map | |
| Filedesc metadata | emd-72009.cif.gz | 7.4 KB | ||
| Others | emd_72009_half_map_1.map.gz emd_72009_half_map_2.map.gz | 226.3 MB 226.3 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-72009 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-72009 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9py5MC ![]() 9pydC ![]() 9pyhC ![]() 9pykC ![]() 9pynC ![]() 9pyyC ![]() 9pz2C ![]() 9pz3C M: atomic model generated by this map C: citing same article ( |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_72009.map.gz / Format: CCP4 / Size: 244.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | sharpened map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.0339 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_72009_msk_1.map | ||||||||||||
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| Density Histograms |
-Half map: half map B
| File | emd_72009_half_map_1.map | ||||||||||||
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| Annotation | half map B | ||||||||||||
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| Density Histograms |
-Half map: half map A
| File | emd_72009_half_map_2.map | ||||||||||||
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| Annotation | half map A | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Q10M-055 Fab in complex with HIV-1 Env Q23 NFL TD CC3+
| Entire | Name: Q10M-055 Fab in complex with HIV-1 Env Q23 NFL TD CC3+ |
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| Components |
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-Supramolecule #1: Q10M-055 Fab in complex with HIV-1 Env Q23 NFL TD CC3+
| Supramolecule | Name: Q10M-055 Fab in complex with HIV-1 Env Q23 NFL TD CC3+ type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3 |
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| Source (natural) | Organism: ![]() Human immunodeficiency virus 1 |
-Macromolecule #1: Q23 NFL TD CC3+ gp140
| Macromolecule | Name: Q23 NFL TD CC3+ gp140 / 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: 72.431008 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: VENLWVTVYY GVPVWRDAET TLFCASDAKA YETEKHNVWA THACVPTDPN PQEIHLDNVT EKFNMWKNNM VEQMHTDIIS LWDQSLKPC VKLTPLCVTL HCTNVTSVNT TGDREGLKNC SFNMTTELRD KRQKVYSLFY RLDIVPINEN QGSEYRLINC N TSAITQAC ...String: VENLWVTVYY GVPVWRDAET TLFCASDAKA YETEKHNVWA THACVPTDPN PQEIHLDNVT EKFNMWKNNM VEQMHTDIIS LWDQSLKPC VKLTPLCVTL HCTNVTSVNT TGDREGLKNC SFNMTTELRD KRQKVYSLFY RLDIVPINEN QGSEYRLINC N TSAITQAC PKVSFEPIPI HYCTPAGFAI LKCKDEGFNG TGLCKNVSTV QCTHGIKPVV STQLLLNGSL AEKNITIRSE NI TNNAKII IVQLVQPVTI KCIRPNNYTR KSIRIGPGQA FYAMGDIIGD IRQAHCNVTR SRWNKTLQEV AEKLRTYFGN KTI IFANSS GGDLEITTHS FNCGGEFFYC NTSGLFNSTW YVNSTWNDTD STQESNDTIT LPCRIKQIIN MWQRAGQAMY APPI PGVIK CESNITGLLL TRDGGKDNNV NETFRPGGGD MRDNWRSELY KYKVVEIEPL GVAPTRCKRR VVEGGGGSGG GGSAV GIGA VRRGFLGAAG STMGATSITL TVQARQLLSG IVQPQNNLLR APEAQQHLLK LGVWGIKQLQ ARVLAVERYL RDQQLL GIW GCSGKLICTT NVPWNSSWSN KSLDEIWNNM TWLQWDKEIG NYTQLIYRLI EESQNQQEKN EKELLCLDGG GGSHHHH HH HHGSGC |
-Macromolecule #2: Q10M-055 Fab heavy chain
| Macromolecule | Name: Q10M-055 Fab heavy chain / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 25.175002 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: QLRLQESGPG LVEPLETLSL TCAVSGGFVS SDYWYWIRQP PGKGLECIGR ISGRHGNTDY SPSLKSRVTI STDTSKNQLS LNLKSVTTA DTAVYYCASD LYYEDD(TYS)GYS YEGLDVFDFW GQGLRVTVSS ASTKGPSVFP LAPSSKSTSG GTAALGC LV KDYFPEPVTV ...String: QLRLQESGPG LVEPLETLSL TCAVSGGFVS SDYWYWIRQP PGKGLECIGR ISGRHGNTDY SPSLKSRVTI STDTSKNQLS LNLKSVTTA DTAVYYCASD LYYEDD(TYS)GYS YEGLDVFDFW GQGLRVTVSS ASTKGPSVFP LAPSSKSTSG GTAALGC LV KDYFPEPVTV SWNSGALTSG VHTFPAVLQS SGLYSLSSVV TVPSSSLGTQ TYICNVNHKP SNTKVDKKVE PKSCDK |
-Macromolecule #3: Q10M-055 Fab light chain
| Macromolecule | Name: Q10M-055 Fab light chain / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 23.415012 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: EIVMTQSPAT LSLSPGERAT LSCRASQSVS YNLAWYQQKP GQAPRLLVYG ASSRATGIPD RFSGSGSGTE FTLTITSLEP EDFAFYFCQ QYIHWPTFGQ GTKVEIKRTV AAPSVFIFPP SDEQLKSGTA SVVCLLNNFY PREAKVQWKV DNALQSGNSQ E SVTEQDSK ...String: EIVMTQSPAT LSLSPGERAT LSCRASQSVS YNLAWYQQKP GQAPRLLVYG ASSRATGIPD RFSGSGSGTE FTLTITSLEP EDFAFYFCQ QYIHWPTFGQ GTKVEIKRTV AAPSVFIFPP SDEQLKSGTA SVVCLLNNFY PREAKVQWKV DNALQSGNSQ E SVTEQDSK DSTYSLSSTL TLSKADYEKH KVYACEVTHQ GLSSPVTKSF NRGEC |
-Macromolecule #9: 2-acetamido-2-deoxy-beta-D-glucopyranose
| Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 9 / Number of copies: 33 / 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
| Concentration | 2.8 mg/mL |
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| Buffer | pH: 7.4 |
| Grid | Model: UltrAuFoil R1.2/1.3 / Material: GOLD / Mesh: 300 / Support film - Material: GOLD / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 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: TFS FALCON 4i (4k x 4k) / Average electron dose: 45.2 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.7 µm / Nominal defocus min: 0.8 µm |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
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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
