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Free keywords:
N-ethylmaleimide sensitive fusion protein; chaperone; soluble NSF attachment protein; SNAP receptor; syntaxin MEMBRANE-FUSION; SYNAPTIC-TRANSMISSION; ENDOPLASMIC-RETICULUM; CRYSTAL-STRUCTURE; BETA-PIX; TERMINAL DOMAIN; GAMMA-SNAP; RECEPTOR; FAMILY; AMPA
Abstract:
N-ethylmaleimide sensitive fusion protein (NSF) is a chaperone that plays a crucial role in the fusion of vesicles with target membranes. NSF mediates the ATP-consuming dissociation of a core protein complex that assembles during vesicle fusion and it thereby recharges the fusion machinery to perform multiple rounds of fusion. The binding of NSF to the core complex is mediated by co-chaperones named soluble NSF attachment proteins (SNAPs), for which three isoforms (alpha, beta and gamma) are known. Here, we sought to identify novel targets of the NSF-SNAP complex. A yeast two-hybrid screen using the brain specific beta SNAP isoform as bait revealed, as expected, NSF and several isoforms of the SNARE protein syntaxin as interactors. In addition, three isoforms of the reticulon protein family and two isoforms of BNIP3 interacted with PS NAP. A yeast two-hybrid screen using NSF as bait identified Rab11-FIP3 and the Pak-binding nucleotide exchange factor PPIX as putative binding partners. PPIX interacts with recombinant NSF in co-sedimentation assays and the two proteins may be co-immunoprecipitated. A leucine zipper (LZ) motif within the C-terminus of beta PIX mediates binding to NSF; however, this fragment of PPIX does not exhibit dominant negative effects in a cellular assay. In summary, our results support the evolving view that NSF has numerous targets in addition to conventional SNARE complexes.
