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Toxins (Basel). 2010 Apr;2(4):665-82. doi: 10.3390/toxins2040665. Epub 2010 Apr 13.

Clostridial neurotoxins: mechanism of SNARE cleavage and outlook on potential substrate specificity reengineering.

Author information

1
Institut für Biochemie, OE 4310, Medizinische Hochschule Hannover, 30623 Hannover, Germany. binz.thomas@mh-hannover.de

Abstract

The clostridial neurotoxin family consists of tetanus neurotoxin and seven distinct botulinum neurotoxins which cause the diseases tetanus and botulism. The extreme potency of these toxins primarily relies not only on their ability to specifically enter motoneurons but also on the activity their catalytic domains display inside presynaptic motoneuronal terminals. Subsequent to neurotoxin binding and endocytosis the catalytic domains become translocated across endosomal membranes and proteolyze unique peptide bonds of one of three soluble N-ethylmaleimide-sensitive fusion protein attachment receptors (SNAREs), vesicle associated membrane protein/synaptobrevin, synaptosome associated protein of 25 kDa, or syntaxin. As these substrate proteins are core components of the vesicular membrane fusion apparatus, cleavage of any of the substrate molecules results in the blockade of neurotransmitter release. This review summarizes the present knowledge about the molecular basis of the specific substrate recognition and cleavage mechanism and assesses the feasibility of reengineering catalytic domains to hydrolyze non-substrate members of the three SNARE families in order to expand the therapeutic application of botulinum neurotoxins.

KEYWORDS:

SNARE; botulinum neurotoxin; enzyme engineering; tetanus toxin; zinc protease

PMID:
22069605
PMCID:
PMC3153214
DOI:
10.3390/toxins2040665
[Indexed for MEDLINE]
Free PMC Article
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