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J Neuroinflammation 9, 112, doi: 10.1186/1742-2094-9-112 (2012)

Furthermore, the dithioamine-Cu2+ complex has been demonstrated to potently inhibit the degradation of ubiquitinated proteins by obstructing upstream signaling pathways of the protease system and suppressing ubiquitination-dependent ATP synthase activity (111)

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We also examined the role of glycosylation by introducing asparagine-to-alanine substitutions at six different potential N -glycosylation sites in surface-targeted LacAnc100, none of which appeared to notably reduce its activity (Supplementary Fig

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