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Yorodumi- EMDB-71417: Gag CA-SP1 immature lattice bound with Lenacapavir from enveloped... -
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Open data
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Basic information
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| Title | Gag CA-SP1 immature lattice bound with Lenacapavir from enveloped virus like particles | |||||||||
Map data | primary map without sharpening | |||||||||
Sample |
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Keywords | HIV-1 / Gag / CA-SP1 / Inhibitor / virion assembly / VIRUS LIKE PARTICLE | |||||||||
| Function / homology | Function and homology informationviral budding via host ESCRT complex / host multivesicular body / ISG15 antiviral mechanism / viral nucleocapsid / viral translational frameshifting / host cell nucleus / host cell plasma membrane / virion membrane / structural molecule activity / RNA binding / zinc ion binding Similarity search - Function | |||||||||
| Biological species | Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.28 Å | |||||||||
Authors | Wu C / Meuser ME / Xiong Y | |||||||||
| Funding support | United States, 2 items
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Citation | Journal: J Am Chem Soc / Year: 2025Title: Distinct Target Site of Lenacapavir in Immature HIV-1 and Concurrent Binding with the Maturation Inhibitor Bevirimat. Authors: Chunxiang Wu / Megan E Meuser / Juan S Rey / Hamed Meshkin / Rachel Yang / Swapnil C Devarkar / Christian Freniere / Jiong Shi / Christopher Aiken / Juan R Perilla / Yong Xiong / ![]() Abstract: HIV-1 inhibitors, such as bevirimat (BVM) and lenacapavir (LEN), significantly reduce the production and maturation of infectious virions. However, their mechanisms remain unclear due to the absence ...HIV-1 inhibitors, such as bevirimat (BVM) and lenacapavir (LEN), significantly reduce the production and maturation of infectious virions. However, their mechanisms remain unclear due to the absence of high-resolution structures for BVM in complex with the immature Gag lattice and LEN's structural data being limited to the mature capsid. Utilizing perforated virus-like particles (VLPs) produced from mammalian cells, we determined in situ cryo-electron microscopy (cryo-EM) structures of HIV-1 with inhibitors. This allowed for the first structural determination of the native immature HIV-1 particle with BVM and LEN bound inside the VLPs at high resolutions. Our findings demonstrate that LEN not only binds the mature capsid but also targets the immature lattice in a distinct manner. The binding of LEN induces a conformational change in the capsid protein (CA) region and alters the architecture of the Gag lattice, which may affect the maturation process. In addition, a more accurate model of BVM engaging the Gag lattice is revealed, one that is independent of LEN binding. These insights expand our understanding of the inhibitory mechanisms of LEN and BVM on HIV-1 and provide valuable clues for the design of future inhibitors. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_71417.map.gz | 67.9 MB | EMDB map data format | |
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| Header (meta data) | emd-71417-v30.xml emd-71417.xml | 26.8 KB 26.8 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_71417_fsc.xml | 11 KB | Display | FSC data file |
| Images | emd_71417.png | 268.1 KB | ||
| Masks | emd_71417_msk_1.map | 144.7 MB | Mask map | |
| Filedesc metadata | emd-71417.cif.gz | 7.3 KB | ||
| Others | emd_71417_additional_1.map.gz emd_71417_half_map_1.map.gz emd_71417_half_map_2.map.gz | 130.1 MB 132.4 MB 132.4 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-71417 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-71417 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9p9lMC ![]() 9cwvC ![]() 9d6cC ![]() 9d6eC ![]() 9d88C ![]() 9dwdC ![]() 9e39C ![]() 9p9mC 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_71417.map.gz / Format: CCP4 / Size: 144.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | primary map without sharpening | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.8942 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_71417_msk_1.map | ||||||||||||
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-Additional map: Sharpened map with B factor of -31.9
| File | emd_71417_additional_1.map | ||||||||||||
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| Annotation | Sharpened map with B factor of -31.9 | ||||||||||||
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-Half map: #2
| File | emd_71417_half_map_1.map | ||||||||||||
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-Half map: #1
| File | emd_71417_half_map_2.map | ||||||||||||
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Sample components
-Entire : Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE)
| Entire | Name: Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE) |
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| Components |
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-Supramolecule #1: Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE)
| Supramolecule | Name: Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE) type: virus / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 Details: NL-MA/NC DNA was transfected into Expi293F (thermofisher) cells and cultured in suspension culture. The enveloped virion like particles were purified by filtration and ultracentrifugation, ...Details: NL-MA/NC DNA was transfected into Expi293F (thermofisher) cells and cultured in suspension culture. The enveloped virion like particles were purified by filtration and ultracentrifugation, and directly used as cryo-EM sample. NCBI-ID: 11698 Sci species name: Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE) Sci species strain: Clone pNL4-3 / Virus type: VIRUS-LIKE PARTICLE / Virus isolate: STRAIN / Virus enveloped: Yes / Virus empty: No |
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| Host (natural) | Organism: Homo sapiens (human) |
| Virus shell | Shell ID: 1 / Name: Gag / Diameter: 1500.0 Å |
-Macromolecule #1: Gag polyprotein
| Macromolecule | Name: Gag polyprotein / type: protein_or_peptide / ID: 1 / Number of copies: 18 / Enantiomer: LEVO |
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| Source (natural) | Organism: Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE)Strain: Clone pNL4-3 |
| Molecular weight | Theoretical: 25.339037 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: VHQAISPRTL NAWVKVVEEK AFSPEVIPMF SALSEGATPQ DLNTMLNTVG GHQAAMQMLK ETINEEAAEW DRLHPVHAGP IAPGQMREP RGSDIAGTTS TLQEQIGWMT HNPPIPVGEI YKRWIILGLN KIVRMYSPTS ILDIRQGPKE PFRDYVDRFY K TLRAEQAS ...String: VHQAISPRTL NAWVKVVEEK AFSPEVIPMF SALSEGATPQ DLNTMLNTVG GHQAAMQMLK ETINEEAAEW DRLHPVHAGP IAPGQMREP RGSDIAGTTS TLQEQIGWMT HNPPIPVGEI YKRWIILGLN KIVRMYSPTS ILDIRQGPKE PFRDYVDRFY K TLRAEQAS QEVKNWMTET LLVQNANPDC KTILKALGPG ATLEEMMTAC QGVGGPGHKA RVIAEAMSQV T UniProtKB: Gag polyprotein |
-Macromolecule #2: Lenacapavir
| Macromolecule | Name: Lenacapavir / type: ligand / ID: 2 / Number of copies: 18 / Formula: QNG |
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| Molecular weight | Theoretical: 968.282 Da |
-Macromolecule #3: INOSITOL HEXAKISPHOSPHATE
| Macromolecule | Name: INOSITOL HEXAKISPHOSPHATE / type: ligand / ID: 3 / Number of copies: 1 / Formula: IHP |
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| Molecular weight | Theoretical: 660.035 Da |
| Chemical component information | ![]() ChemComp-IHP: |
-Macromolecule #4: water
| Macromolecule | Name: water / type: ligand / ID: 4 / Number of copies: 90 / Formula: HOH |
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| Molecular weight | Theoretical: 18.015 Da |
| Chemical component information | ![]() ChemComp-HOH: |
-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 mg/mL | ||||||||||||
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| Buffer | pH: 7.4 Component:
Details: This is the final buffer in which the enveloped viral like particle was resuspended. The Gag-CA-SP1 lattice is inside the viral like particle and thus not in the direct environment of this buffer. | ||||||||||||
| Grid | Model: Quantifoil R2/1 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 30 sec. / Details: 15mA current | ||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK III | ||||||||||||
| Details | NL-MA/NC DNA was transfected into Expi293F (thermofisher) cells and cultured in suspension culture. The enveloped virion like particles were purified by filtration and ultracentrifugation, and directly used as cryo-EM sample. |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Software | Name: SerialEM |
| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.2 µm / Nominal defocus min: 1.2 µm / Nominal magnification: 81000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE)
Keywords
Authors
United States, 2 items
Citation

















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Y (Row.)
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Homo sapiens (human)

Processing
FIELD EMISSION GUN

