Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2064199 | Toxicon | 2016 | 6 Pages |
Abstract
During cellular uptake, diphtheria toxin delivers its catalytic domain DTA from acidified endosomes into the cytosol, which requires reduction of the disulfide linking DTA to the transport domain. In vitro, thioredoxin reduces this disulfide and thioredoxin reductase (TrxR) is part of a cytosolic complex facilitating DTA-translocation. We found that the TrxR-specific inhibitor auranofin prevented DTA delivery into the cytosol and intoxication of HeLa cells with diphtheria toxin, offering perspectives for novel pharmacological strategies against diphtheria.
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Authors
Leonie Schnell, Lydia Dmochewitz-Kück, Peter Feigl, Cesare Montecucco, Holger Barth,