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Neutralisation of specific surface carboxylates speeds up translocation of botulinum neurotoxin type B enzymatic domain.

Authors :
Pirazzini M
Henke T
Rossetto O
Mahrhold S
Krez N
Rummel A
Montecucco C
Binz T
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.)

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