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Structures of neurexophilin-neurexin complexes reveal a regulatory mechanism of alternative splicing.

Steven C Wilson | K Ian White | Qiangjun Zhou | Richard A Pfuetzner | Ucheor B Choi | Thomas C Südhof | Axel T Brunger
The EMBO journal | 2019

Neurexins are presynaptic, cell-adhesion molecules that specify the functional properties of synapses via interactions with trans-synaptic ligands. Neurexins are extensively alternatively spliced at six canonical sites that regulate multifarious ligand interactions, but the structural mechanisms underlying alternative splicing-dependent neurexin regulation are largely unknown. Here, we determined high-resolution structures of the complex of neurexophilin-1 and the second laminin/neurexin/sex-hormone-binding globulin domain (LNS2) of neurexin-1 and examined how alternative splicing at splice site #2 (SS2) regulates the complex. Our data reveal a unique, extensive, neurexophilin-neurexin binding interface that extends the jelly-roll β-sandwich of LNS2 of neurexin-1 into neurexophilin-1. The SS2A insert of LNS2 augments this interface, increasing the binding affinity of LNS2 for neurexophilin-1. Taken together, our data reveal an unexpected architecture of neurexophilin-neurexin complexes that accounts for the modulation of binding by alternative splicing, which in turn regulates the competition of neurexophilin for neurexin binding with other ligands.

Pubmed ID: 31566781

Research resources used in this publication

None found

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Associated grants

  • Agency: Stanford Genome Training Program, International
    Id: 4T32HG000044-20
  • Agency: Stanford Genome Training Program, International
    Id: 2T32HG000044-21
  • Agency: Howard Hughes Medical Institute (HHMI), International
  • Agency: NIH HHS, United States
    Id: S10 OD021512
  • Agency: NIMH NIH HHS, United States
    Id: R37 MH052804
  • Agency: Stanford Genome Training Program, International
    Id: 5T32HG000044-19
  • Agency: NIMH NIH HHS, United States
    Id: R37 MH063105
  • Agency: HHS | National Institutes of Health (NIH), International
    Id: R37MH63105
  • Agency: National Institute of General Medical Sciences from the National Institutes of Health, International
    Id: P41GM103393

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