| Literature DB >> 25911959 |
Leonie Schnell1, Lydia Dmochewitz-Kück1, Peter Feigl1, Cesare Montecucco2, Holger Barth3.
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.Entities:
Keywords: Auranofin; Cellular uptake; Diphtheria toxin; Endosome; Membrane translocation; Thioredoxin reductase
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Year: 2015 PMID: 25911959 DOI: 10.1016/j.toxicon.2015.04.012
Source DB: PubMed Journal: Toxicon ISSN: 0041-0101 Impact factor: 3.033