Abstract
Nerve growth factor (NGF) receptor binding, internalisation and transportation of NGF has been identified as a potential route of delivery for other molecules. A derivative of Clostridium botulinum neurotoxin type A (LH(N)) that retains catalytic activity but has significantly reduced cell-binding capability has been prepared and chemically coupled to NGF. Intact clostridial neurotoxins potently inhibit neurotransmitter release at the neuromuscular junction by proteolysis of specific components of the vesicle docking/fusion complex. Here we report that the NGF-LH(N)/A conjugate, when applied to PC12 cells, significantly inhibited neurotransmitter release and cleaved the type A toxin substrate. This work represents the successful use of NGF as a targeting moiety for the delivery of a neurotoxin fragment.
Original language | English |
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Pages (from-to) | 147-155 |
Number of pages | 9 |
Journal | Growth Factors |
Volume | 18 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2000 |
Keywords
- Botulinum toxin type A
- Nerve growth factor
- PC12 cells
- Synaptosomal-associated protein 25