Anthrax toxin: receptor binding, internalization, pore formation, and translocation

Annu Rev Biochem. 2007:76:243-65. doi: 10.1146/annurev.biochem.75.103004.142728.

Abstract

Anthrax toxin consists of three nontoxic proteins that self-assemble at the surface of receptor-bearing mammalian cells or in solution, yielding a series of toxic complexes. Two of the proteins, called Lethal Factor (LF) and Edema Factor (EF), are enzymes that act on cytosolic substrates. The third, termed Protective Antigen (PA), is a multifunctional protein that binds to receptors, orchestrates the assembly and internalization of the complexes, and delivers them to the endosome. There, the PA moiety forms a pore in the endosomal membrane and promotes translocation of LF and EF to the cytosol. Recent advances in understanding the entry process include insights into how PA recognizes its two known receptors and its ligands, LF and EF; how the PA:receptor interaction influences the pH-dependence of pore formation; and how the pore functions in promoting translocation of LF and EF across the endosomal membrane.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens, Bacterial / chemistry*
  • Antigens, Bacterial / genetics
  • Antigens, Bacterial / metabolism*
  • Bacterial Toxins / chemistry*
  • Bacterial Toxins / genetics
  • Bacterial Toxins / metabolism*
  • Binding Sites
  • Endocytosis / physiology*
  • Furin / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Membrane Microdomains / metabolism
  • Membrane Proteins / chemistry*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Microfilament Proteins
  • Models, Molecular
  • Mutation
  • Neoplasm Proteins / chemistry*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Phenylalanine / chemistry
  • Phenylalanine / metabolism
  • Pore Forming Cytotoxic Proteins / chemistry
  • Pore Forming Cytotoxic Proteins / metabolism
  • Protein Binding
  • Protein Conformation
  • Protein Subunits / chemistry
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • Receptors, Cell Surface / chemistry*
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*
  • Receptors, Peptide

Substances

  • ANTXR1 protein, human
  • ANTXR2 protein, human
  • Antigens, Bacterial
  • Bacterial Toxins
  • Membrane Proteins
  • Microfilament Proteins
  • Neoplasm Proteins
  • Pore Forming Cytotoxic Proteins
  • Protein Subunits
  • Receptors, Cell Surface
  • Receptors, Peptide
  • anthrax toxin
  • Phenylalanine
  • Furin