Membrane topologies of neuronal SNARE folding intermediates

Biochemistry. 2002 Sep 10;41(36):10928-33. doi: 10.1021/bi026266v.

Abstract

Assembly of the SNARE complex is essential for neurotransmitter release at synapses. Target plasma membrane SNAREs (t-SNAREs) syntaxin 1A and SNAP-25 form the t-SNARE complex that serves as an intermediate toward final SNARE assembly with vesicle-associated SNARE (v-SNARE). Membrane topologies of syntaxin 1A and the t-SNARE complex were investigated using site-directed spin labeling EPR. EPR analysis revealed that the basic region at the membrane-water interface is unstructured but inserted into the membrane. Such membrane insertion leaves no gap between the t-SNARE core and the membrane. Yet the lack of structure could provide the flexibility necessary for the t-SNARE core. Further, the insertion of the basic interfacial region into the membrane may have profound implications for the mechanism of SNARE-induced membrane fusion.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Antigens, Surface / chemistry
  • Dimerization
  • Electron Spin Resonance Spectroscopy / methods
  • Membrane Fusion / physiology
  • Membrane Proteins / chemistry*
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nerve Tissue Proteins / chemistry
  • Neurons / chemistry*
  • Peptide Fragments / chemistry
  • Peptide Fragments / physiology
  • Protein Folding*
  • SNARE Proteins
  • Spin Labels
  • Syntaxin 1
  • Vesicular Transport Proteins*

Substances

  • Antigens, Surface
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Peptide Fragments
  • SNARE Proteins
  • Spin Labels
  • Syntaxin 1
  • Vesicular Transport Proteins