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Yorodumi- EMDB-19518: IFTB1 (proximal region) in retrograde Intraflagellar transport trains -
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Open data
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Basic information
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| Title | IFTB1 (proximal region) in retrograde Intraflagellar transport trains | |||||||||
Map data | Overall unfiltered map | |||||||||
Sample |
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Keywords | Cilia / IFT / train / retrograde / PROTEIN TRANSPORT | |||||||||
| Biological species | ![]() | |||||||||
| Method | subtomogram averaging / cryo EM / Resolution: 18.05 Å | |||||||||
Authors | Lacey SE / Pigino G | |||||||||
| Funding support | European Union, 2 items
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Citation | Journal: Cell / Year: 2024Title: Extensive structural rearrangement of intraflagellar transport trains underpins bidirectional cargo transport. Authors: Samuel E Lacey / Andrea Graziadei / Gaia Pigino / ![]() Abstract: Bidirectional transport in cilia is carried out by polymers of the IFTA and IFTB protein complexes, called anterograde and retrograde intraflagellar transport (IFT) trains. Anterograde trains deliver ...Bidirectional transport in cilia is carried out by polymers of the IFTA and IFTB protein complexes, called anterograde and retrograde intraflagellar transport (IFT) trains. Anterograde trains deliver cargoes from the cell to the cilium tip, then convert into retrograde trains for cargo export. We set out to understand how the IFT complexes can perform these two directly opposing roles before and after conversion. We use cryoelectron tomography and in situ cross-linking mass spectrometry to determine the structure of retrograde IFT trains and compare it with the known structure of anterograde trains. The retrograde train is a 2-fold symmetric polymer organized around a central thread of IFTA complexes. We conclude that anterograde-to-retrograde remodeling involves global rearrangements of the IFTA/B complexes and requires complete disassembly of the anterograde train. Finally, we describe how conformational changes to cargo-binding sites facilitate unidirectional cargo transport in a bidirectional system. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_19518.map.gz | 7.8 MB | EMDB map data format | |
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| Header (meta data) | emd-19518-v30.xml emd-19518.xml | 14.9 KB 14.9 KB | Display Display | EMDB header |
| Images | emd_19518.png | 13.6 KB | ||
| Masks | emd_19518_msk_1.map | 10.5 MB | Mask map | |
| Filedesc metadata | emd-19518.cif.gz | 4.1 KB | ||
| Others | emd_19518_additional_1.map.gz emd_19518_half_map_1.map.gz emd_19518_half_map_2.map.gz | 68.4 KB 7.9 MB 7.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-19518 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-19518 | 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_19518.map.gz / Format: CCP4 / Size: 10.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Overall unfiltered map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 6.06 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_19518_msk_1.map | ||||||||||||
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-Additional map: The main map after Locspiral filtering and masking....
| File | emd_19518_additional_1.map | ||||||||||||
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| Annotation | The main map after Locspiral filtering and masking. This was then used for composite map generation | ||||||||||||
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-Half map: #2
| File | emd_19518_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_19518_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : In situ retrograde intraflagellar transport trains in dhc1b-3 mut...
| Entire | Name: In situ retrograde intraflagellar transport trains in dhc1b-3 mutant Chlamydomonas reinhardtii cilia |
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| Components |
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-Supramolecule #1: In situ retrograde intraflagellar transport trains in dhc1b-3 mut...
| Supramolecule | Name: In situ retrograde intraflagellar transport trains in dhc1b-3 mutant Chlamydomonas reinhardtii cilia type: cell / ID: 1 / Parent: 0 Details: Temperature sensitive cells incubated at restrictive temperature (34 degrees C) for 10 hours and plunge frozen on grids. |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | subtomogram averaging |
| Aggregation state | cell |
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Sample preparation
| Buffer | pH: 7 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: TFS FALCON 4i (4k x 4k) / Average electron dose: 2.6 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 4.0 µm / Nominal defocus min: 2.0 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Final reconstruction | Applied symmetry - Point group: C2 (2 fold cyclic) / Resolution.type: BY AUTHOR / Resolution: 18.05 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION (ver. 3.1.3) / Number subtomograms used: 3177 |
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| Extraction | Number tomograms: 756 / Number images used: 10455 |
| CTF correction | Software - Name: CTFFIND (ver. 4) / Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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FIELD EMISSION GUN
