Evidence for a conserved inhibitory binding mode between the membrane fusion assembly factors Munc18 and syntaxin in animals

Morey, C; Kienle, CN; Klöpper, TH; Burkhardt, P; Fasshauer, D. 2017 Evidence for a conserved inhibitory binding mode between the membrane fusion assembly factors Munc18 and syntaxin in animals. Journal of Biological Chemistry, 292 (50). 20449-20460. 10.1074/jbc.M117.811182

[img] Text
J. Biol. Chem.-2017-Morey-jbc.M117.811182.pdf - Published Version
Restricted to Repository staff only until 18 October 2018.
Available under License All Rights Reserved.

Download (1MB)
Official URL: https://doi.org/10.1074/jbc.M117.811182

Abstract/Summary

The membrane fusion necessary for vesicle trafficking is driven by the assembly of heterologous SNARE proteins orchestrated by the binding of Sec1/Munc18 (SM) proteins to specific syntaxin SNARE proteins. However, the precise mode of interaction between SM proteins and SNAREs is debated, as contrasting binding modes have been found for different members of the SM protein family, including the three vertebrate Munc18 isoforms. While different binding modes could be necessary given their roles in different secretory processes in different tissues, the structural similarity of the three isoforms makes this divergence perplexing. Though the neuronal isoform Munc18a is well established to bind tightly to both the closed conformation and the N-peptide of Syntaxin 1a, thereby inhibiting SNARE complex formation, Munc18b and c, which have a more widespread distribution, are reported to mainly interact with the N-peptide of their partnering syntaxins and are thought to instead promote SNARE complex formation. We have re-investigated the interaction between Munc18c and Syntaxin 4 (Syx4). Using isothermal titration calorimetry, we found that Munc18c, like Munc18a, binds to both the closed conformation and the N-peptide of Syx4. Furtermore, using a novel kinetic approach, we found that Munc18c, like Munc18a, slows down SNARE complex formation through high-affinity binding to syntaxin. This strongly suggests that secretory Munc18s in general control the accessibility of the bound syntaxin, probably preparing it for SNARE complex assembly.

Item Type: Publication - Article
Divisions: Marine Biological Association of the UK > Mechanisms underlying biogeochemical and ecological processes > Cell and Molecular Programme
Depositing User: Barbara Bultmann
Date made live: 17 Jan 2018 11:48
Last Modified: 17 Jan 2018 11:48
URI: http://plymsea.ac.uk/id/eprint/7691

Actions (login required)

View Item View Item