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Yorodumi- EMDB-72208: Cryo EM structure of elk ACE2 in complex with XBB 1.5 spike RBD -
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Open data
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Basic information
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| Title | Cryo EM structure of elk ACE2 in complex with XBB 1.5 spike RBD | |||||||||
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Keywords | SARS-CoV-2 / Cervidae / ACE2 receptor / viral host interaction / host susceptibility / VIRAL PROTEIN | |||||||||
| Biological species | ![]() ![]() Severe acute respiratory syndrome coronavirus | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.3 Å | |||||||||
Authors | Ye K / Tao YJ / Wan XF | |||||||||
| Funding support | United States, 2 items
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Citation | Journal: Nat Commun / Year: 2026Title: Species- and variant-specific ACE2 compatibility shapes SARS-CoV-2 spillover potential in North American cervids. Authors: Constanza Espada / Kai Ye / Yingyi Long / Kritika Pasai / Thomas J DeLiberto / Jonathon Heale / Riley Wiese / Qiongying Yang / Mingyi Zhou / Sean Streich / Yizhi Jane Tao / Jeffrey C Chandler / Xiu-Feng Wan / ![]() Abstract: Free-ranging white-tailed deer (WTD) are established SARS-CoV-2 reservoirs, but the susceptibility of other cervid species remains unclear. Here we integrate receptor analysis, structural modeling, ...Free-ranging white-tailed deer (WTD) are established SARS-CoV-2 reservoirs, but the susceptibility of other cervid species remains unclear. Here we integrate receptor analysis, structural modeling, and field surveillance to assess SARS-CoV-2 susceptibility across North American cervids. We identify species- and variant-specific differences in ACE2-spike compatibility. Elk ACE2 exhibits weak binding to the ancestral strain (Wuhan-Hu-1) and Delta spike receptor-binding domains (RBDs), likely due to a unique K31N substitution. In contrast, it shows stronger binding to Alpha, Beta, Gamma, and Omicron RBDs containing N501Y. Biophysical assays, gel filtration chromatography, and cryo-EM confirm stable complex formation between elk ACE2 and Alpha RBD, but not RBD from the ancestral strain. Despite weak binding, elk ACE2 supports viral entry and replication in vitro. However, surveillance revealed limited evidence of infection in the United States, contrasting with widespread WTD transmissions. These findings demonstrate that ACE2 compatibility alone is insufficient to predict reservoir potential and provide a framework for assessing species susceptibility to emerging coronaviruses. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_72208.map.gz | 777.8 MB | EMDB map data format | |
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| Header (meta data) | emd-72208-v30.xml emd-72208.xml | 25.8 KB 25.8 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_72208_fsc.xml | 19.9 KB | Display | FSC data file |
| Images | emd_72208.png | 129.1 KB | ||
| Masks | emd_72208_msk_1.map | 824 MB | Mask map | |
| Filedesc metadata | emd-72208.cif.gz | 7.6 KB | ||
| Others | emd_72208_half_map_1.map.gz emd_72208_half_map_2.map.gz | 765.5 MB 765.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-72208 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-72208 | 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_72208.map.gz / Format: CCP4 / Size: 824 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: 0.832 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_72208_msk_1.map | ||||||||||||
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-Half map: #2
| File | emd_72208_half_map_1.map | ||||||||||||
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-Half map: #1
| File | emd_72208_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Binary complex of elk ACE2 with SARS-CoV-2 XBB 1.5 Spike RBD
| Entire | Name: Binary complex of elk ACE2 with SARS-CoV-2 XBB 1.5 Spike RBD |
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| Components |
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-Supramolecule #1: Binary complex of elk ACE2 with SARS-CoV-2 XBB 1.5 Spike RBD
| Supramolecule | Name: Binary complex of elk ACE2 with SARS-CoV-2 XBB 1.5 Spike RBD type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 Details: This complex is from local refinement of the elk ACE2:spike complex |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 35 KDa |
-Supramolecule #2: Elk ACE2 extracellular domain
| Supramolecule | Name: Elk ACE2 extracellular domain / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #2 |
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| Source (natural) | Organism: ![]() |
-Supramolecule #3: Receptor binding domain of SARS-CoV-2 XBB1.5 spike protein
| Supramolecule | Name: Receptor binding domain of SARS-CoV-2 XBB1.5 spike protein type: complex / ID: 3 / Parent: 1 / Macromolecule list: #1 |
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| Source (natural) | Organism: Severe acute respiratory syndrome coronavirus |
-Macromolecule #1: Spike protein
| Macromolecule | Name: Spike protein / type: protein_or_peptide / ID: 1 Details: Author stated the sequence reference should be GB XBC18596.1 Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 25.159553 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: RVQPTESIVR FPNITNLCPF HEVFNATTFA SVYAWNRKRI SNCVADYSVI YNFAPFFAFK CYGVSPTKLN DLCFTNVYAD SFVIRGNEV SQIAPGQTGN IADYNYKLPD DFTGCVIAWN SNKLDSKPSG NYNYLYRLFR KSKLKPFERD ISTEIYQAGN K PCNGVAGP ...String: RVQPTESIVR FPNITNLCPF HEVFNATTFA SVYAWNRKRI SNCVADYSVI YNFAPFFAFK CYGVSPTKLN DLCFTNVYAD SFVIRGNEV SQIAPGQTGN IADYNYKLPD DFTGCVIAWN SNKLDSKPSG NYNYLYRLFR KSKLKPFERD ISTEIYQAGN K PCNGVAGP NCYSPLQSYG FRPTYGVGHQ PYRVVVLSFE LLHAPATVCG PKKSTNLVKN KCVNF |
-Macromolecule #2: Angiotensin-converting enzyme 2
| Macromolecule | Name: Angiotensin-converting enzyme 2 / type: protein_or_peptide / ID: 2 Details: Author stated the sequence reference should be GB XP_043314478.1 Number of copies: 1 / Enantiomer: LEVO / EC number: Hydrolases; Acting on peptide bonds (peptidases) |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 72.4425 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MTGSFWLLLS LVAVTAAQST TEEQAKTFLE NFNHEAEDLS YQSSLASWNY NTNITDENVQ KMNEARAKWS AFYEEQSRMA KTYSLEEIQ NLTLKRQLKA LQQSGTSVLS AEKSKRLNTI LNTMSTIYST GKVLDPNTQE CLALEPGLDD IMENSRDYNR R LWAWEGWR ...String: MTGSFWLLLS LVAVTAAQST TEEQAKTFLE NFNHEAEDLS YQSSLASWNY NTNITDENVQ KMNEARAKWS AFYEEQSRMA KTYSLEEIQ NLTLKRQLKA LQQSGTSVLS AEKSKRLNTI LNTMSTIYST GKVLDPNTQE CLALEPGLDD IMENSRDYNR R LWAWEGWR AEVGKQLRPL YEEYVVLENE MARANNYEDY GDYWRGDYEV TEAGDYDYSR DQLMKDVEHT FAEIKPLYEQ LH AYVRAKL MDTYPSYISP TGCLPAHLLG DMWGRFWTNL YSLTVPFKHK PSIDVTEKME NQSWDAERIF KEAEKFFVSI GLP HMTQGF WDNSMLTEPG DGRKVVCHPT AWDLGKGDFR IKMCTKVTMD DFLTAHHEMG HIQYDMAYAA QPYLLRNGAN EGFH EAVGE IMSLSAATPH YLKALGLLEP DFYEDNETEI NFLLKQALTI VGTLPFTYML EKWRWMVFKG EIPKEQWMQK WWEMK REIV GVVEPLPHDE TYCDPACLFH VAEDYSFIRY YTRTIYQFQF HEALCKTAKH EGALFKCDIS NSTEAGQRLL QMLSLG KSE PWTLALESIV GIKTMDVKPL LNYFEPLFTW LKEQNKNSFV GWSTEWTPYS DGGHHHHHH |
-Macromolecule #3: 2-acetamido-2-deoxy-beta-D-glucopyranose
| Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 3 / Number of copies: 4 / 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 | 1.8 mg/mL |
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| Buffer | pH: 7.4 / Details: 1x PBS, pH 7.4 |
| Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 400 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. / Pretreatment - Atmosphere: AIR / Pretreatment - Pressure: 0.05 kPa Details: The grids were glow discharged with the current set to be 30 mA. |
| Vitrification | Cryogen name: ETHANE |
| Details | Elk ACE2 and SARS-CoV-2 omicron XBB1.5 spike protein samples were mixed at a 3:1 molar ratio at 1.8 mg/ml total protein concentration for 2 hr at 4 oC. |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Number grids imaged: 3 / Average electron dose: 1.25 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Calibrated defocus max: 3.0 µm / Calibrated defocus min: 0.8 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 105000 |
| 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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Keywords

Authors
United States, 2 items
Citation


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Processing
FIELD EMISSION GUN


