Generation of nonidentical compartments in vesicular transport systems

J Cell Biol. 2005 Jan 17;168(2):271-80. doi: 10.1083/jcb.200409087.

Abstract

How can organelles communicate by bidirectional vesicle transport and yet maintain different protein compositions? We show by mathematical modeling that a minimal system, in which the basic variables are cytosolic coats for vesicle budding and membrane-bound soluble N-ethyl-maleimide-sensitive factor attachment protein receptors (SNAREs) for vesicle fusion, is sufficient to generate stable, nonidentical compartments. A requirement for establishing and maintaining distinct compartments is that each coat preferentially packages certain SNAREs during vesicle budding. Vesicles fuse preferentially with the compartment that contains the highest concentration of cognate SNAREs, thus further increasing these SNAREs. The stable steady state is the result of a balance between this autocatalytic SNARE accumulation in a compartment and the distribution of SNAREs between compartments by vesicle budding. The resulting nonhomogeneous SNARE distribution generates coat-specific vesicle fluxes that determine the size of compartments. With nonidentical compartments established in this way, the localization and cellular transport of cargo proteins can be explained simply by their affinity for coats.

Publication types

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

MeSH terms

  • Algorithms
  • COP-Coated Vesicles / metabolism
  • COP-Coated Vesicles / physiology
  • Endoplasmic Reticulum / metabolism
  • Endosomes / metabolism
  • Eukaryotic Cells / physiology
  • Golgi Apparatus / metabolism
  • Intracellular Membranes / metabolism
  • Intracellular Membranes / physiology
  • Membrane Fusion / physiology
  • Models, Biological*
  • Protein Transport / physiology
  • SNARE Proteins
  • Transport Vesicles / physiology*
  • Vesicular Transport Proteins / metabolism
  • Vesicular Transport Proteins / physiology

Substances

  • SNARE Proteins
  • Vesicular Transport Proteins