Journal Article10.1152/PHYSREV.2000.80.2.717
Neurotoxins Affecting Neuroexocytosis
TL;DR: The mechanism of action of three groups of presynaptic neurotoxins that interfere directly with the process of neurotransmitter release is reviewed, whereas presynapses acting on ion channels are not dealt with here.
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Abstract: Nerve terminals are specific sites of action of a very large number of toxins produced by many different organisms. The mechanism of action of three groups of presynaptic neurotoxins that interfere directly with the process of neurotransmitter release is reviewed, whereas presynaptic neurotoxins acting on ion channels are not dealt with here. These neurotoxins can be grouped in three large families: 1) the clostridial neurotoxins that act inside nerves and block neurotransmitter release via their metalloproteolytic activity directed specifically on SNARE proteins; 2) the snake presynaptic neurotoxins with phospholipase A(2) activity, whose site of action is still undefined and which induce the release of acethylcholine followed by impairment of synaptic functions; and 3) the excitatory latrotoxin-like neurotoxins that induce a massive release of neurotransmitter at peripheral and central synapses. Their modes of binding, sites of action, and biochemical activities are discussed in relation to the symptoms of the diseases they cause. The use of these toxins in cell biology and neuroscience is considered as well as the therapeutic utilization of the botulinum neurotoxins in human diseases characterized by hyperfunction of cholinergic terminals.
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Citations
Studies on the dissociation of botulinum neurotoxin type A complexes.
TL;DR: BoNT A toxin complexes have evolved to quickly respond to specific environmental changes by efficient release of the neurotoxin by effecting the quantitative dissociation of 900 kDa complexes and release of free neurotoxin prior to injection into target tissues.
159
Reversible Suppression of Glutamatergic Neurotransmission of Cerebellar Granule Cells In Vivo by Genetically Manipulated Expression of Tetanus Neurotoxin Light Chain
Mutsuya Yamamoto,Norio Wada,Yasuji Kitabatake,Dai Watanabe,Masayuki Anzai,Minesuke Yokoyama,Yutaka Teranishi,Shigetada Nakanishi +7 more
TL;DR: Reversible suppression of glutamatergic neurotransmission can be manipulated with spatiotemporal accuracy by DOX treatment and removal and will serve as an animal model to study the cerebellar function in motor coordination and learning.
Molecular mechanisms of active zone function
TL;DR: The structure and function of the active zone is discussed, which is defined as the region of the presynapse that is specialized for vesicle release and particular emphasis is put on the molecular players that control spatial restriction, efficiency and timing of exocytosis in the mammalian nervous system.
159
Botulinum neurotoxins C, E and F bind gangliosides via a conserved binding site prior to stimulation‐dependent uptake with botulinum neurotoxin F utilising the three isoforms of SV2 as second receptor
Andreas Rummel,Kirstin Häfner,Stefan Mahrhold,Natallia Darashchonak,Matthew Holt,Reinhard Jahn,Silke Beermann,Tino Karnath,Hans Bigalke,Thomas Binz +9 more
TL;DR: It is demonstrated that BoNT/F as wells depends on the presence of gangliosides, by employing phrenic nerve hemidiaphragm preparations derived from mice expressing GM3, GM2, GM1 and GD1a or only GM3.
158
Distinct Kinetic Changes in Neurotransmitter Release After SNARE Protein Cleavage
TL;DR: A difference between BoNT/C1 and TeNT emerged, which suggests that cleavage of synaptobrevin modifies the coupling between channels and release-competent vesicles when stimulating release by calcium influx through channels.
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TL;DR: The X-ray crystal structure of a core synaptic fusion complex containing syntaxin-1A, synaptobrevin-II and SNAP-25B reveals a highly twisted and parallel four-helix bundle that differs from the bundles described for the haemagglutinin and HIV/SIV gp41 membrane-fusion proteins.
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Mechanisms of intracellular protein transport
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