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Neutralisation of specific surface carboxylates speeds up translocation of botulinum neurotoxin type B enzymatic domain.
- Source :
-
FEBS letters [FEBS Lett] 2013 Nov 29; Vol. 587 (23), pp. 3831-6. Date of Electronic Publication: 2013 Oct 21. - Publication Year :
- 2013
-
Abstract
- Botulinum neurotoxins translocate their enzymatic domain across vesicular membranes. The molecular triggers of this process are unknown. Here, we tested the possibility that this is elicited by protonation of conserved surface carboxylates. Glutamate-48, glutamate-653 and aspartate-877 were identified as possible candidates and changed into amide. This triple mutant showed increased neurotoxicity due to faster cytosolic delivery of the enzymatic domain; membrane translocation could take place at less acidic pH. Thus, neutralisation of specific negative surface charges facilitates membrane contact permitting a faster initiation of the toxin membrane insertion.<br /> (Copyright © 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Aspartic Acid chemistry
Aspartic Acid genetics
Botulinum Toxins genetics
Botulinum Toxins metabolism
Botulinum Toxins toxicity
Botulinum Toxins, Type A
Cells, Cultured
Cytosol metabolism
Glutamic Acid chemistry
Glutamic Acid genetics
Hydrogen-Ion Concentration
Mice
Mutation
Neurons drug effects
Neurotoxins chemistry
Neurotoxins genetics
Neurotoxins metabolism
Neurotoxins toxicity
Protein Transport
Botulinum Toxins chemistry
Catalytic Domain
Cell Membrane metabolism
Protons
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3468
- Volume :
- 587
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 24157364
- Full Text :
- https://doi.org/10.1016/j.febslet.2013.10.010