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Self-delivery of evolved proteases into cancer cells To harness the self-delivery capabilities of BoNT proteases, we expressed and purified evolved proteases X(PC) and X(GD) as fusions with the wild-type BoNT/X translocation domain (H N )
These observations strongly support the current hypothesis that reactive metabolite formation and protein binding especially in mitochondria are the key initiating events in the toxicity, which is then the trigger for a moderate mitochondrial oxidant stress with release of superoxide by complex III towards the cytosol without compromise of mitochondrial respiration [33]
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