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- EMDB-45259: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex con... -

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Basic information

Entry
Database: EMDB / ID: EMD-45259
TitleIn-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map
Map dataIn-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map
Sample
  • Cell: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map
KeywordsNuclear envelope / Nuclear pore / Nucleocytoplasmic transport / STRUCTURAL PROTEIN
Biological speciesToxoplasma gondii RH (eukaryote)
Methodsubtomogram averaging / cryo EM / Resolution: 57.0 Å
AuthorsSingh D / Hutchings J / Li Z / Guo Q / Villa E
Funding support United States, European Union, 4 items
OrganizationGrant numberCountry
Howard Hughes Medical Institute (HHMI) United States
Damon Runyon Cancer Research FoundationDRG-2364-19 United States
European Molecular Biology Organization (EMBO)ALTF 871-2020European Union
National Institutes of Health/National Institute on Aging (NIH/NIA)K99AG080112 United States
CitationJournal: Cell / Year: 2024
Title: The molecular architecture of the nuclear basket.
Authors: Digvijay Singh / Neelesh Soni / Joshua Hutchings / Ignacia Echeverria / Farhaz Shaikh / Madeleine Duquette / Sergey Suslov / Zhixun Li / Trevor van Eeuwen / Kelly Molloy / Yi Shi / Junjie ...Authors: Digvijay Singh / Neelesh Soni / Joshua Hutchings / Ignacia Echeverria / Farhaz Shaikh / Madeleine Duquette / Sergey Suslov / Zhixun Li / Trevor van Eeuwen / Kelly Molloy / Yi Shi / Junjie Wang / Qiang Guo / Brian T Chait / Javier Fernandez-Martinez / Michael P Rout / Andrej Sali / Elizabeth Villa /
Abstract: The nuclear pore complex (NPC) is the sole mediator of nucleocytoplasmic transport. Despite great advances in understanding its conserved core architecture, the peripheral regions can exhibit ...The nuclear pore complex (NPC) is the sole mediator of nucleocytoplasmic transport. Despite great advances in understanding its conserved core architecture, the peripheral regions can exhibit considerable variation within and between species. One such structure is the cage-like nuclear basket. Despite its crucial roles in mRNA surveillance and chromatin organization, an architectural understanding has remained elusive. Using in-cell cryo-electron tomography and subtomogram analysis, we explored the NPC's structural variations and the nuclear basket across fungi (yeast; S. cerevisiae), mammals (mouse; M. musculus), and protozoa (T. gondii). Using integrative structural modeling, we computed a model of the basket in yeast and mammals that revealed how a hub of nucleoporins (Nups) in the nuclear ring binds to basket-forming Mlp/Tpr proteins: the coiled-coil domains of Mlp/Tpr form the struts of the basket, while their unstructured termini constitute the basket distal densities, which potentially serve as a docking site for mRNA preprocessing before nucleocytoplasmic transport.
History
DepositionJun 8, 2024-
Header (metadata) releaseAug 21, 2024-
Map releaseAug 21, 2024-
UpdateOct 2, 2024-
Current statusOct 2, 2024Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

emd_45259.png

Downloads & links

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Map

FileDownload / File: emd_45259.map.gz / Format: CCP4 / Size: 30.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationIn-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map
Projections & slices

Image control

Size
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AxesZ (Sec.)Y (Row.)X (Col.)
10 Å/pix.
x 200 pix.
= 2000. Å		10 Å/pix.
x 200 pix.
= 2000. Å		10 Å/pix.
x 200 pix.
= 2000. Å

Surface

Projections

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Slices (1/2)

Slices (2/3)

Images are generated by Spider.

Voxel sizeX=Y=Z: 10 Å
Density

Histogram

Histogram (log scale)
Contour LevelBy AUTHOR: 0.671
Minimum - Maximum-0.85462165 - 1.3667957
Average (Standard dev.)0.021876965 (±0.19037147)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions200200200
Spacing200200200
CellA=B=C: 2000.0 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_45259_msk_1.map
Projections & Slices
AxesZYX

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Slices (1/2)
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Half map: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus...

Fileemd_45259_half_map_1.map
AnnotationIn-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map - half map 1
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

Histogram

Histogram (log scale)

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Half map: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus...

Fileemd_45259_half_map_2.map
AnnotationIn-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map - half map 2
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

Histogram

Histogram (log scale)

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Sample components

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Entire : In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex con...

EntireName: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map
Components
  • Cell: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map

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Supramolecule #1: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex con...

SupramoleculeName: In-cell Toxoplasma gondii C8-symmetrised nuclear pore complex consensus map
type: cell / ID: 1 / Parent: 0
Source (natural)Organism: Toxoplasma gondii RH (eukaryote)

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Experimental details

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Structure determination

Methodcryo EM
Processingsubtomogram averaging
Aggregation statecell

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Sample preparation

BufferpH: 7
VitrificationCryogen name: ETHANE / Instrument: FEI VITROBOT MARK IV

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Image recordingFilm or detector model: GATAN K3 (6k x 4k) / Detector mode: COUNTING / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Average electron dose: 3.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 5.0 µm / Nominal defocus min: 3.0 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Final reconstructionApplied symmetry - Point group: C8 (8 fold cyclic) / Resolution.type: BY AUTHOR / Resolution: 57.0 Å / Resolution method: FSC 0.143 CUT-OFF / Number subtomograms used: 40
ExtractionNumber tomograms: 19 / Number images used: 50
Final angle assignmentType: MAXIMUM LIKELIHOOD

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