9si1 | pdb_00009si1

Mouse otoferlin (216-1931) in the lipid-free Ca2+-bound state, "closed-like" conformation

spinqualitylabelsall models 9si1, resolution 3.10Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9si1 is a 1 chain structure with sequence from Mus musculus. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Electron Microscopy, Resolution 3.1Å Ligands: CA Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function A0A0R4J1K2_MOUSE Key calcium ion sensor involved in the Ca(2+)-triggered synaptic vesicle-plasma membrane fusion and in the control of neurotransmitter release at these output synapses. Interacts in a calcium-dependent manner to the presynaptic SNARE proteins at ribbon synapses of cochlear inner hair cells (IHCs) to trigger exocytosis of neurotransmitter. Also essential to synaptic exocytosis in immature outer hair cells (OHCs). May also play a role within the recycling of endosomes.[ARBA:ARBA00056096] Publication Abstract from PubMed Hearing relies upon speedy synaptic transmission of sound information from inner hair cells (IHCs) to spiral ganglion neurons. To accomplish this, IHCs use a sophisticated presynaptic machinery including the multi-C(2) domain protein otoferlin that is affected by human deafness mutations. Otoferlin is essential for IHC exocytosis, but how it binds Ca(2+) and the target membrane to serve synaptic vesicle (SV) tethering, docking, and fusion remained unclear. Here, we obtained cryo-electron microscopy structures of otoferlin and employed molecular dynamics simulations of membrane binding. We show that membrane binding by otoferlin involves C(2)B-C(2)G domains and repositions C(2)F and C(2)G domains. Disruption of Ca(2+)-binding sites of the C(2)D domain in mice altered synaptic sound encoding and eliminated the Ca(2+) cooperativity of IHC exocytosis, indicating that it requires the binding of several Ca(2+)-ions by otoferlin. Together, our findings elucidate molecular mechanisms underlying otoferlin-mediated SV docking and support the role of otoferlin as Ca(2+) sensor of SV fusion in IHCs. Structure and function of otoferlin, a synaptic protein of sensory hair cells essential for hearing.,Chen H, Cretu C, Trebilcock A, Evdokimova N, Babai N, Feldmann L, Leidner F, Benseler F, Mutschall S, Esch K, Szabo CZK, Pena V, Pape C, Grubmuller H, Strenzke N, Brose N, Wichmann C, Preobraschenski J, Moser T Sci Adv. 2025 Oct 17;11(42):eady8532. doi: 10.1126/sciadv.ady8532. Epub 2025 Oct , 15. PMID:41091875 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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