Evidence for a Proton–Protein Symport Mechanism in the Anthrax Toxin Channel

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Evidence for a Proton–Protein Symport Mechanism in the Anthrax Toxin Channel

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Title: Evidence for a Proton–Protein Symport Mechanism in the Anthrax Toxin Channel
Author: Basilio, Daniel; Juris, Stephen J.; Finkelstein, Alan; Collier, R. John

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Citation: Basilio, Daniel, Stephen J. Juris, R. John Collier, and Alan Finkelstein. 2009. Evidence for a proton–protein symport mechanism in the anthrax toxin channel. Journal of General Physiology 133(3): 307-314.
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Abstract: The toxin produced by Bacillus anthracis, the causative agent of anthrax, is composed of three proteins: a translocase heptameric channel, (PA\(_{63})_7\), formed from protective antigen (PA), which allows the other two proteins, lethal and edema factors (LF and EF), to translocate across a host cell's endosomal membrane, disrupting cellular homeostasis. It has been shown that (PA\(_{63})_7\) incorporated into planar phospholipid bilayer membranes forms a channel capable of transporting LF and EF. Protein translocation through the channel is driven by a proton electrochemical potential gradient on a time scale of seconds. A paradoxical aspect of this is that although LFN (the N-terminal 263 residues of LF), on which most of our experiments were performed, has a net negative charge, it is driven through the channel by a cis-positive voltage. We have explained this by claiming that the (PA\(_{63})_7\) channel strongly disfavors the entry of negatively charged residues on proteins to be translocated, and hence the aspartates and glutamates on LF\(_\text{N}\) enter protonated (i.e., neutralized). Therefore, the translocated species is positively charged. Upon exiting the channel, the protons that were picked up from the cis solution are released into the trans solution, thereby making this a proton–protein symporter. Here, we provide further evidence of such a mechanism by showing that if only one SO\(_3^−\), which is essentially not titratable, is introduced at most positions in LF\(_\text{N}\), through the reaction of an introduced cysteine residue at those positions with 2-sulfonato-ethyl-methanethiosulfonate, voltage-driven LF\(_\text{N}\) translocation is drastically inhibited. We also find that a site that disfavors the entry of negatively charged residues into the (PA\(_{63})_7\) channel resides at or near its Φ-clamp, the ring of seven phenylalanines near the channel's entrance.
Published Version: doi:10.1085/jgp.200810170
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654084/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8347340
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