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9OKC

22bin20S complex (NSF-alphaSNAP-2:2 syntaxin-1a:SNAP-25), hydrolyzing, class 17

Summary for 9OKC
Entry DOI10.2210/pdb9okc/pdb
Related9OJ2 9OJJ 9OJR 9OJU 9OJZ 9OK3 9OK5
EMDB information70559
DescriptorVesicle-fusing ATPase, Undefined N-terminus of SNAP-25 or syntaxin-1a, ADENOSINE-5'-DIPHOSPHATE, ... (6 entities in total)
Functional Keywordsatpase, snare, hydrolysis, disassembly, translocation, exocytosis, neurotransmitter release, synapse, synaptic transmission, membrane fusion, hydrolase
Biological sourceCricetulus griseus (Chinese hamster)
More
Total number of polymer chains7
Total formula weight504583.63
Authors
White, K.I.,Brunger, A.T. (deposition date: 2025-05-09, release date: 2025-08-06, Last modification date: 2025-10-08)
Primary citationWhite, K.I.,Khan, Y.A.,Qiu, K.,Balaji, A.,Couoh-Cardel, S.,Esquivies, L.,Pfuetzner, R.A.,Diao, J.,Brunger, A.T.
Structural remodeling of target-SNARE protein complexes by NSF enables synaptic transmission.
Nat Commun, 16:8371-8371, 2025
Cited by
PubMed Abstract: Synaptic vesicles containing neurotransmitters fuse with the plasma membrane upon the arrival of an action potential at the active zone. Multiple proteins organize trans-SNARE complex assembly and priming, leading to fusion. One target membrane SNARE, syntaxin, forms nanodomains at the active zone, and another, SNAP-25, enters non-fusogenic complexes with it. Here, we reveal mechanistic details of AAA+ protein NSF (N-ethylmaleimide sensitive factor) and SNAP (soluble NSF attachment protein) action before fusion. We show that syntaxin clusters are conserved, that NSF colocalizes with them, and characterize SNARE populations that may exist within or near them using cryo-EM. Supercomplexes of NSF, α-SNAP, and either a syntaxin tetramer or one of two binary complexes of syntaxin-SNAP-25 reveal atomic details of SNARE processing and show how sequential ATP hydrolysis drives disassembly. These results suggest a functional role for syntaxin clusters as reservoirs and a corresponding role for NSF in syntaxin liberation and SNARE protein quality control preceding fusion.
PubMed: 40993127
DOI: 10.1038/s41467-025-62764-0
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.67 Å)
Structure validation

244349

數據於2025-11-05公開中

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