Abstract
Anthrax toxin consists of three proteins (approx. 90kDa each): lethal factor (LF); oedema factor (OF); and protective antigen (PA). The former two are enzymes that act when they reach the cytosol of a targeted cell. To enter the cytosol, however, which they do after being endocytosed into an acidic vesicle compartment, they require the third component, PA. PA (or rather its proteolytically generated fragment PA63) forms at low pH a heptameric beta-barrel channel, (PA63)7, through which LF and OF are transported--a phenomenon we have demonstrated in planar phospholipid bilayers. It might appear that (PA63)7 simply forms a large hole through which LF and OF diffuse. However, LF and OF are folded proteins, much too large to fit through the approximately 15A diameter (PA63)7 beta-barrel. This paper discusses how the (PA63)7 channel both participates in the unfolding of LF and OF and functions in their translocation as a proton-protein symporter.
MeSH Terms
Antigens, Bacterial/chemistry,metabolism
Bacillus anthracis/metabolism
Bacterial Toxins/chemistry,metabolism
Hydrogen-Ion Concentration
Models, Molecular
Protein Conformation
Protein Folding
Protein Transport/physiology
Protons
Chemicals
Antigens, Bacterial
Bacterial Toxins
Protons
anthrax toxin
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Finkelstein Alan
Departments of Physiology and Biophysics and Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA. alfinkel@aecom.yu.edu
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