rsly1 binding to syntaxin 5 is required for endoplasmic reticulum-to-Golgi transport but does not promote SNARE motif accessibility

Mol Biol Cell. 2004 Jan;15(1):162-75. doi: 10.1091/mbc.e03-07-0535. Epub 2003 Oct 17.

Abstract

Although some of the principles of N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) function are well understood, remarkably little detail is known about sec1/munc18 (SM) protein function and its relationship to SNAREs. Popular models of SM protein function hold that these proteins promote or maintain an open and/or monomeric pool of syntaxin molecules available for SNARE complex formation. To address the functional relationship of the mammalian endoplasmic reticulum/Golgi SM protein rsly1 and its SNARE binding partner syntaxin 5, we produced a conformation-specific monoclonal antibody that binds only the available, but not the cis-SNARE-complexed nor intramolecularly closed form of syntaxin 5. Immunostaining experiments demonstrated that syntaxin 5 SNARE motif availability is nonuniformly distributed and focally regulated. In vitro endoplasmic reticulum-to-Golgi transport assays revealed that rsly1 was acutely required for transport, and that binding to syntaxin 5 was absolutely required for its function. Finally, manipulation of rsly1-syntaxin 5 interactions in vivo revealed that they had remarkably little impact on the pool of available syntaxin 5 SNARE motif. Our results argue that although rsly1 does not seem to regulate the availability of syntaxin 5, its function is intimately associated with syntaxin binding, perhaps promoting a later step in SNARE complex formation or function.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Carrier Proteins / metabolism*
  • Cells, Cultured
  • Cloning, Molecular
  • Endoplasmic Reticulum / metabolism*
  • Golgi Apparatus / metabolism*
  • Immediate-Early Proteins / metabolism*
  • Membrane Proteins / metabolism*
  • Microscopy, Fluorescence
  • Models, Molecular
  • Munc18 Proteins
  • Protein Binding / drug effects
  • Protein Structure, Tertiary / physiology
  • Protein Transport / physiology
  • Qa-SNARE Proteins
  • Rats
  • SNARE Proteins
  • Vesicular Transport Proteins*

Substances

  • Antibodies, Monoclonal
  • Carrier Proteins
  • Immediate-Early Proteins
  • Membrane Proteins
  • Munc18 Proteins
  • Qa-SNARE Proteins
  • SNARE Proteins
  • Scfd1 protein, rat
  • Vesicular Transport Proteins