Structure of alpha-latrotoxin oligomers reveals that divalent cation-dependent tetramers form membrane pores

Nat Struct Biol. 2000 Jan;7(1):48-53. doi: 10.1038/71247.

Abstract

We report here the first three-dimensional structure of alpha-latrotoxin, a black widow spider neurotoxin, which forms membrane pores and stimulates secretion in the presence of divalent cations. We discovered that alpha-latrotoxin exists in two oligomeric forms: it is dimeric in EDTA but forms tetramers in the presence of Ca2+ or Mg2+. The dimer and tetramer structures were determined independently at 18 A and 14 A resolution, respectively, using cryo-electron microscopy and angular reconstitution. The alpha-latrotoxin monomer consists of three domains. The N- and C-terminal domains have been identified using antibodies and atomic fitting. The C4-symmetric tetramers represent the active form of alpha-latrotoxin; they have an axial channel and can insert into lipid bilayers with their hydrophobic base, providing the first model of alpha-latrotoxin pore formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Black Widow Spider / chemistry*
  • Calcium / pharmacology
  • Cations, Divalent / pharmacology*
  • Cryoelectron Microscopy
  • Dimerization
  • Edetic Acid / pharmacology
  • Magnesium / pharmacology
  • Membrane Proteins / chemistry*
  • Membrane Proteins / ultrastructure*
  • Models, Molecular
  • Molecular Sequence Data
  • Molecular Weight
  • Norepinephrine / metabolism
  • Presynaptic Terminals / drug effects
  • Presynaptic Terminals / metabolism
  • Protein Denaturation
  • Protein Renaturation / drug effects
  • Protein Structure, Quaternary / drug effects*
  • Protein Structure, Tertiary
  • Sequence Alignment
  • Spider Venoms / chemistry*
  • Spider Venoms / pharmacology
  • Structure-Activity Relationship

Substances

  • Cations, Divalent
  • Membrane Proteins
  • Spider Venoms
  • alpha-latrotoxin
  • Edetic Acid
  • Magnesium
  • Calcium
  • Norepinephrine