4.7 Article

Toward the discovery of dual inhibitors for botulinum neurotoxin A: concomitant targeting of endocytosis and light chain protease activity

期刊

CHEMICAL COMMUNICATIONS
卷 51, 期 28, 页码 6226-6229

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc00677e

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  1. National Institute of Health [AI080671]
  2. Fulbright Commission
  3. Scripps Research Institute [29038]

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Dyngo-4a (TM) has been found to be an endocytic inhibitor of BoNT/A neurotoxicity through dynamin inhibition. Herein, we demonstrate this molecule to have a previously unrecognized dual activity against BoNT/A, dynamin-protease inhibition. To establish the importance of this dual activity, detailed kinetic analysis of Dyngo-4a's inhibition of BoNT/A metalloprotease as well as cellular and animal toxicity studies have been described. The research presented is the first polypharmacological approach to counteract BoNT/A intoxication.

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