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Open data
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Basic information
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Title | Cryo-EM structure of the dimeric Elapor1 mutant | |||||||||
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![]() | Tethering factor / MEMBRANE PROTEIN | |||||||||
Function / homology | ![]() positive regulation of autophagosome assembly / autophagosome assembly / cellular response to starvation / trans-Golgi network / late endosome / lysosome / plasma membrane Similarity search - Function | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.6 Å | |||||||||
![]() | Ma J / Zheng S | |||||||||
Funding support | ![]()
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![]() | ![]() Title: ELAPOR1 is a copper-dependent tethering factor driving proacrosomal vesicle fusion during acrosome biogenesis. Authors: Tianyu Shao / Jiahao Ma / Xinshui Tan / Hongcheng Shan / Dan Xu / Kexin Zhang / Sanduo Zheng / Fengchao Wang / ![]() Abstract: The acrosome is a crucial organelle essential for sperm function and male fertility. During acrosome biogenesis, numerous proacrosomal vesicles (PAVs) are transported to the concave region of the ...The acrosome is a crucial organelle essential for sperm function and male fertility. During acrosome biogenesis, numerous proacrosomal vesicles (PAVs) are transported to the concave region of the nuclear membrane and fuse to form the acrosome. However, the mechanisms governing the fusion of PAVs to form the acrosome remain poorly understood. Here, we identify endosome-lysosome associated apoptosis and autophagy regulator 1 (ELAPOR1), a conserved protein, as a key factor in PAVs fusion during acrosome biogenesis. Male mice lacking () are infertile, exhibiting defective acrosome biogenesis and a globozoospermia-like phenotype. Using cryo-electron microscopy revealed that ELAPOR1 forms a square planar homodimer in cis, which assembles into a trans-tetramer via head-to-head homophilic interactions dependent on copper chelation. Notably, ELAPOR1 exhibits dual membrane orientation, with a predicted N - C topology and a noncanonical N - C topology in vesicles. The noncanonical N - C topology enables ELAPOR1 to function as a tethering factor bridging vesicles through head-to-head homophilic interactions. A mutant ELAPOR1 (ELAPOR1) incapable of copper chelation forms cis homodimers but fails to mediate homophilic interactions in vitro, leading to defective PAVs fusion in mice, phenocopying the -deficient mice. Additionally, ELAPOR1 was shown to interact with soluble N-ethylmaleimide sensitive factor attachment protein receptors protein STX12. Conditional knockout of in germ cells resulted in similar defects in acrosome biogenesis. Collectively, our findings suggest that ELAPOR1 functions as a tethering factor that regulates PAV fusion through a copper-dependent mechanism. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
Map data | ![]() | 97.2 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 18.4 KB 18.4 KB | Display Display | ![]() |
Images | ![]() | 72.5 KB | ||
Filedesc metadata | ![]() | 6.6 KB | ||
Others | ![]() ![]() | 95.5 MB 95.5 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 817.7 KB | Display | ![]() |
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Full document | ![]() | 817.2 KB | Display | |
Data in XML | ![]() | 13.4 KB | Display | |
Data in CIF | ![]() | 15.8 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 9vqlMC ![]() 9vqmC M: atomic model generated by this map C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
EMDB pages | ![]() ![]() |
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Related items in Molecule of the Month |
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Map
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Voxel size | X=Y=Z: 1.087 Å | ||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
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Sample components
-Entire : Elapor1 mutant
Entire | Name: Elapor1 mutant |
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Components |
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-Supramolecule #1: Elapor1 mutant
Supramolecule | Name: Elapor1 mutant / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: ![]() ![]() |
-Macromolecule #1: Endosome/lysosome-associated apoptosis and autophagy regulator 1
Macromolecule | Name: Endosome/lysosome-associated apoptosis and autophagy regulator 1 type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 110.429422 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MKTIIALSYI FCLVFADYKD DDDKGSHHHH HHSGMGPELA ACKESEYAFE YTACDSTGSR WRVAVPASPG LCTSLPDPVK GTECSFSCN AGEFLDMKDQ SCKPCAEGRY SLGTGIRFDE WDELPHGFAS LSANLEVDDS ISESTENCTS SKWVPRGDYI A SNTDECTA ...String: MKTIIALSYI FCLVFADYKD DDDKGSHHHH HHSGMGPELA ACKESEYAFE YTACDSTGSR WRVAVPASPG LCTSLPDPVK GTECSFSCN AGEFLDMKDQ SCKPCAEGRY SLGTGIRFDE WDELPHGFAS LSANLEVDDS ISESTENCTS SKWVPRGDYI A SNTDECTA TLMYAVNLKQ SGTVNFEYYY PDSSIIFEFF VQNDQCQPSA DDSRWMKTTE KGWEFHSVEL NRGNNVLYWR TT AFSVWSK VSKPVLVRNI AITGVAYTSE CFPCKPGTYA AKQGSPFCKL CPANYYSNKG ETSCAPCDAD KYSEKGSSTC KVR PACTDK DYFYTHTACD AQGETQLMYK WAIPKICGED LEGAVKLPAS GVKTRCPPCN PGFFKTDNST CEPCPYGSYS NGSD CTHCP AGTEPAVGFE YKWWNTLPSN METTVLSGIN FEYKGLTGWE VAGDHIYTAV GASDNDFMIL TLVVPGFRPP QSVVA DTEN KEVARITFVF ETICSVNCEL YFMVGMNSRT NTPVETWKGT KGKQSYTYTI EENATVSFTW AFQRTTLHET GRKYTN DVA KIYSINVTNV MGGVASYCRP CALEASDLGS SCTSCPAGHY INRDSGTCHL CPSNTILKAH QPYGAQACVP CGPGTKN NK IHSLCYNDCT FSRNTPSRIF NYNFSALAGT VSLAGVPSFT SKGLKYFHHF TLSLCGNQGK KMAVCTDNVT DLRIPDGE A GFSKSVTAYV CQVVIIPSEV MGYKAGVSSQ PVSLADRLVG VSTDMTLEGI VSPVELFHPE TSGIPDIVFF FRSNDVTQS CSSGRSTTIR LRCNPMKAAP GTLRLPSMCS DGTCDGCNFH FLWESVAACP LCSASDYHTF VSSCVAGIQK TTYMWREPKL CSGGISLPE QRVTICKTID FWLKVGISAG TCTAILLTVL TCYFWKKNQK LEYKYSKLVM NATLKDCDLP AADSCAIMEG E DVEDDFIF TSKKSLFGKI KSFTSKRTPD GFDSVPLKTS SGGPDMDM UniProtKB: Endosome/lysosome-associated apoptosis and autophagy regulator 1 |
-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: 6 / 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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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.4 |
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TALOS ARCTICA |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.8 µm / Nominal defocus min: 1.6 µm |
Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |