Literature DB >> 35810329

Stability profile of the neuronal SNARE complex reflects its potency to drive fast membrane fusion.

Shen Wang1, Cong Ma2.   

Abstract

Soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) form the SNARE complex to mediate most fusion events of the secretory pathway. The neuronal SNARE complex is featured by its high stability and half-zippered conformation required for driving robust and fast synaptic exocytosis. However, these two features seem to be thermodynamically mutually exclusive. In this study, we have employed temperature-dependent disassociation assays and single-molecule Förster resonance energy transfer (FRET) experiments to analyze the stability and conformation of the neuronal SNARE complex. We reclassified the amino acids of the SNARE motif into four sub-groups (core, core-side I and II, and non-contact). Our data showed that the core residues predominantly contribute to the complex stability to meet a basal requirement for SNARE-mediated membrane fusion, while the core-side residues exert an unbalanced effect on the N- and C-half bundle stability that determines the half-zippered conformation of the neuronal SNARE complex, which would accommodate essential regulations by complexins and synaptotagmins for fast Ca2+-triggered membrane fusion. Furthermore, our data confirmed a strong coupling of folding energy between the N- and C-half assembly of the neuronal SNARE complex, which rationalizes the strong potency of the half-zippered conformation to conduct robust and fast fusion. Overall, these results uncovered that the stability profile of the neuronal SNARE complex reflects its potency to drive fast and robust membrane fusion. Based on these results, we also developed a new parameter, the stability factor (Fs), to characterize the overall stability of the neuronal SNARE complex and resolved a linear correlation between the stability and inter-residue coulombic interactions of the neuronal SNARE complex, which would help rationally design artificial SNARE complexes and remold functional SNARE complexes with desirable stability.
Copyright © 2022 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2022        PMID: 35810329      PMCID: PMC9463651          DOI: 10.1016/j.bpj.2022.07.013

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   3.699


  85 in total

1.  Homo- and heterooligomeric SNARE complexes studied by site-directed spin labeling.

Authors:  M Margittai; D Fasshauer; S Pabst; R Jahn; R Langen
Journal:  J Biol Chem       Date:  2001-01-19       Impact factor: 5.157

2.  SNARE assembly and disassembly exhibit a pronounced hysteresis.

Authors:  Dirk Fasshauer; Wolfram Antonin; Vinod Subramaniam; Reinhard Jahn
Journal:  Nat Struct Biol       Date:  2002-02

3.  High resolution structure, stability, and synaptotagmin binding of a truncated neuronal SNARE complex.

Authors:  James A Ernst; Axel T Brunger
Journal:  J Biol Chem       Date:  2002-12-20       Impact factor: 5.157

4.  SNAREing the basis of multicellularity: consequences of protein family expansion during evolution.

Authors:  Tobias H Kloepper; C Nickias Kienle; Dirk Fasshauer
Journal:  Mol Biol Evol       Date:  2008-07-10       Impact factor: 16.240

5.  SNARE proteins: one to fuse and three to keep the nascent fusion pore open.

Authors:  Lei Shi; Qing-Tao Shen; Alexander Kiel; Jing Wang; Hong-Wei Wang; Thomas J Melia; James E Rothman; Frédéric Pincet
Journal:  Science       Date:  2012-03-16       Impact factor: 47.728

6.  Fusion Protein Targeted Antiviral Peptides: Fragment-Based Drug Design (FBDD) Guided Rational Design of Dipeptides Against SARS-CoV-2.

Authors:  Sounik Manna; Trinath Chowdhury; Piyush Baindara; Santi M Mandal
Journal:  Curr Protein Pept Sci       Date:  2020       Impact factor: 3.272

7.  Dissecting the disulphide-coupled folding pathway of bovine pancreatic trypsin inhibitor. Forming the first disulphide bonds in analogues of the reduced protein.

Authors:  N J Darby; T E Creighton
Journal:  J Mol Biol       Date:  1993-08-05       Impact factor: 5.469

8.  The structure of the yeast plasma membrane SNARE complex reveals destabilizing water-filled cavities.

Authors:  Pavel Strop; Stephen E Kaiser; Marija Vrljic; Axel T Brunger
Journal:  J Biol Chem       Date:  2007-10-22       Impact factor: 5.157

Review 9.  SNARE complexes and neuroexocytosis: how many, how close?

Authors:  Cesare Montecucco; Giampietro Schiavo; Sergio Pantano
Journal:  Trends Biochem Sci       Date:  2005-07       Impact factor: 13.807

10.  Common intermediates and kinetics, but different energetics, in the assembly of SNARE proteins.

Authors:  Sylvain Zorman; Aleksander A Rebane; Lu Ma; Guangcan Yang; Matthew A Molski; Jeff Coleman; Frederic Pincet; James E Rothman; Yongli Zhang
Journal:  Elife       Date:  2014-09-01       Impact factor: 8.140

View more
  1 in total

1.  Rabphilin 3A binds the N-peptide of SNAP-25 to promote SNARE complex assembly in exocytosis.

Authors:  Tianzhi Li; Qiqi Cheng; Shen Wang; Cong Ma
Journal:  Elife       Date:  2022-09-29       Impact factor: 8.713

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.