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- EMDB-55811: Deconvolved piDPC tomogram of lift-out lamellae from cell-derived... -

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Basic information

Entry
Database: EMDB / ID: EMD-55811
TitleDeconvolved piDPC tomogram of lift-out lamellae from cell-derived matrices
Map dataDeconvolved piDPC tomogram of lift-out lamellae from cell-derived matrices
Sample
  • Cell: TIFF fibroblast cells
KeywordsMitochondrial morphology / whole cell tomography / cryo-STEM Tomography / CSTET / UNKNOWN FUNCTION
Biological speciesHomo sapiens (human)
Methodelectron tomography / cryo EM
AuthorsKirchweger P / Seifer S / Wolf SG / Zens B / Schur FKM / Elbaum M
Funding support Israel, European Union, United States, 4 items
OrganizationGrant numberCountry
Israel Science Foundation1696/18 Israel
European Union (EU)IMpaCT (grant no.857203)European Union
European Research Council (ERC)101055413European Union
Chan Zuckerberg InitiativeDAF2021-234754 United States
CitationJournal: Biorxiv / Year: 2025
Title: Azimuthal Segment Imaging in cryo-STEM Tomography
Authors: Kirchweger P / Seifer S / Wolf SG / Varsano N / Zens B / Schur FK / Elbaum M
History
DepositionNov 24, 2025-
Header (metadata) releaseDec 17, 2025-
Map releaseDec 17, 2025-
UpdateDec 17, 2025-
Current statusDec 17, 2025Processing site: PDBe / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_55811.map.gz / Format: CCP4 / Size: 5.1 GB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationDeconvolved piDPC tomogram of lift-out lamellae from cell-derived matrices
Projections & slices

Image control

Size
Brightness
Contrast
Others
AxesZ (Sec.)Y (Row.)X (Col.)
21.62 Å/pix.
x 347 pix.
= 7502.14 Å
21.62 Å/pix.
x 1980 pix.
= 42807.602 Å
21.62 Å/pix.
x 1981 pix.
= 42829.223 Å

Projections

Slices (1/3)

Slices (1/2)

Slices (2/3)

Images are generated by Spider.

generated in cubic-lattice coordinate

Voxel sizeX=Y=Z: 21.62 Å
Density
Minimum - Maximum-767.500999999999976 - 35596.19999999999709
Average (Standard dev.)6387.763700000000426 (±2186.277599999999893)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin250-215
Dimensions19801981347
Spacing19811980347
CellA: 42829.223 Å / B: 42807.6 Å / C: 7502.14 Å
α=β=γ: 90.0 °

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Supplemental data

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Sample components

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Entire : TIFF fibroblast cells

EntireName: TIFF fibroblast cells
Components
  • Cell: TIFF fibroblast cells

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Supramolecule #1: TIFF fibroblast cells

SupramoleculeName: TIFF fibroblast cells / type: cell / ID: 1 / Parent: 0 / Details: cell-derivet matrix
Source (natural)Organism: Homo sapiens (human)

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Experimental details

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Structure determination

Methodcryo EM
Processingelectron tomography
Aggregation statecell

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Sample preparation

BufferpH: 7.4 / Details: DMEM growth media
GridModel: Quantifoil R2/2 / Support film - Material: CARBON / Support film - topology: HOLEY
VitrificationCryogen name: ETHANE
High pressure freezingInstrument: OTHER
Details: The value given for _em_high_pressure_freezing.instrument is BAL-TEC HPM010. This is not in a list of allowed values {'EMS-002 RAPID IMMERSION FREEZER', 'OTHER', 'LEICA EM PACT2', 'LEICA EM ...Details: The value given for _em_high_pressure_freezing.instrument is BAL-TEC HPM010. This is not in a list of allowed values {'EMS-002 RAPID IMMERSION FREEZER', 'OTHER', 'LEICA EM PACT2', 'LEICA EM PACT', 'LEICA EM HPM100', 'BAL-TEC HPM 010'} so OTHER is written into the XML file.
SectioningFocused ion beam - Instrument: OTHER / Focused ion beam - Ion: OTHER / Focused ion beam - Voltage: 30 / Focused ion beam - Current: 0.5 / Focused ion beam - Duration: 10 / Focused ion beam - Temperature: 100 K / Focused ion beam - Initial thickness: 3000 / Focused ion beam - Final thickness: 900
Focused ion beam - Details: Cryo-lift-out lamellae were generated using a second-generation Aquilos (Aquilos II) instrument (Thermo Fisher Scientific). The instrument was operated using the xT user ...Focused ion beam - Details: Cryo-lift-out lamellae were generated using a second-generation Aquilos (Aquilos II) instrument (Thermo Fisher Scientific). The instrument was operated using the xT user interface and the MAPS 3.14 software (TFS). The FIB was operated at 30 kV, and the milling progress was monitored using the SEM beam at 25 pA and 5 kV. A 45deg pretilt shuttle was used for all cryo-FIB milling steps described below. Prior to sample loading, a 100/400 rectangular mesh grid (#G1040-Cu; Science Services) was clipped into an AutoGrid as receiver grid. For clipping, the long side of the rectangle mesh was placed perpendicular to the milling window to allow for easy lift-out attachment and low-angle sample thinning. After loading the sample and receiver grid, overview maps of the high-pressure frozen specimens were acquired and correlated with the images acquired on a Leica EM Cryo CLEM microscope to identify regions of interest. The milling slot on the FIBSEM AutoGrid was used to improve correlation by using its rim, visible in both reflected light microscopy and SEM, as a landmark. The specimen was cleaned from contaminations such as debris and ice in eucentric position at 20deg stage tilt with the FIB operated at 1 nA. Directing the beam to areas with contamination facilitates its removal to create a smooth, clean surface for subsequent coatings. The specimen was sputter-coated with platinum for 30 s at 30 mA and 10 Pa with the built-in sputter coater, followed by a GIS deposition of 1.5 to 2 um metalorganic platinum and another sputter-coating (30s, 30mA, 10 Pa). Tile-scan overview images were taken after each step using the MAPS software. Lift-out sites were identified by CLEM and set to eucentric position. Steps performed for the lift-out FIB milling are explained in greater detailed in Zens et al (2024): Trenches for the lift-out procedure were cut at a stage tilt of 7deg and a relative stage rotation of 180deg to position the FIB perpendicular to the sample. The trenches in front, behind, and to the side of the lift-out were milled in cross-section (CS) patterns with 5 nA. The front and back of the lift-out were polished smooth by milling with cross-section-cleaning (CSC) patterns fitted to the width of the lift-out with 1 nA. Undercuts were performed at 28deg stage tilt, at the default stage rotation, with 1 nA with rectangle milling patterns. The micromanipulator needle was then attached by redeposition milling, using a CS pattern with a Multi-Pass setting of 1 at 0.5 nA. The remaining anchor to the bulk sample was removed at 0.5 nA with a rectangle pattern placed at the anchor position. The lift-out was then lifted out of the bulk sample and transferred to the receiver grid. The grid bars at the attachment site were pre-milled at default stage rotation, 22deg stage tilt, with a CS pattern and a current of 15 nA. The patterns were set up to produce an angled recess matching the width of the lift-out and a z-depth of ~15um. This ensured a better attachment of the lift-out as well as a pre-tilt close to the desired final milling angle. The lift-out was then attached to this recess at eucentric height at a relative stage rotation of 180deg and a stage tilt of 22deg. The lift-out block was maneuvered into the pre-milled slot before attachment by redeposition milling, using CS patterns at 0.5 nA with a Multi-Pass setting of 1, a z-depth of 3 um, and an area of roughly2/1.5 um (x/y). Following visual confirmation of the attachment, the needle was pulled off gently to the side, so it could be directly reused for the next lift-out without any necessary cleaning steps. Each lift-out was then thinned with rectangle patterns to in several steps, reducing lamella width and milling current in each step, resulting in a symmetric stair-like anchor. Final lamella width was approximately 20 um. Lamellae were thinned down to 3 um thickness with 1 nA, then to 1.5 um thickness with 0.5 nA, and to 900 nm using 0.1 nA. Here, the stage was tilted to plus/minus 1deg and the lamella overhangs above and below were milled with 0.1 nA to facilitate a parallel shape of the lamella rather than a wedge-like one. The lamellae were then milled down to 600-900 nm with 50 pA.. The value given for _em_focused_ion_beam.instrument is Aquilos II. This is not in a list of allowed values {'DB235', 'OTHER'} so OTHER is written into the XML file.

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Electron microscopy

MicroscopeTFS TALOS
Image recordingFilm or detector model: OTHER / Digitization - Dimensions - Width: 4096 pixel / Digitization - Dimensions - Height: 4096 pixel / Average exposure time: 50.0 sec. / Average electron dose: 4.0 e/Å2
Electron beamAcceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN
Electron opticsC2 aperture diameter: 50.0 µm / Calibrated defocus min: 0.0 µm / Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 0.0 µm / Nominal defocus min: 0.0 µm / Nominal magnification: 28500
Sample stageCooling holder cryogen: NITROGEN

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Image processing

Final reconstructionAlgorithm: BACK PROJECTION
Software:
Namedetails
IMOD (ver. 4.12.10)
PRIISM/IVE (ver. 4.7.2)Deconvolved using core2_decon

Number images used: 53
CTF correctionDetails: CSTET needs no CTF correction / Type: NONE

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