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
Use of botulinum toxins in cancer therapy.
Réginald Ansiaux,Bernard Gallez +1 more
TL;DR: It can be seen that BoNTs act by an effect on the tumour microenvironment rather than by a direct cytotoxic effect on tumour cells, allowing more effective destruction of cancer cells by radiotherapy and chemotherapy.
Calcium-dependent Regulation of SNARE-mediated Membrane Fusion by Calmodulin
Jerome Di Giovanni,Jerome Di Giovanni,Cécile Iborra,Cécile Iborra,Yves Maulet,Yves Maulet,Christian Lévêque,Christian Lévêque,Oussama El Far,Oussama El Far,Michael Seagar,Michael Seagar +11 more
TL;DR: Findings suggest that two distinct Ca2+ sensors act antagonistically in SNARE-mediated fusion, and that synaptotagmin displaced calmodulin binding to target-SNAREs.
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Site-directed mutagenesis identifies active-site residues of the light chain of botulinum neurotoxin type A.
TL;DR: Mutation of the Glu-262* nearly abolishes SNAP-25 hydrolysis as expected for a residue involved in zinc coordination and of a tyrosine and a phenylalanine residues that occupy critical positions within the active site of BoNT/A are presented.
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Adrenergic and cholinergic activity contributes to the cardiovascular effects of lionfish (Pterois volitans) venom
Jarrod E Church,Wayne C. Hodgson +1 more
TL;DR: It is concluded that P. volitans venom produces its cardiovascular effects primarily by acting on muscarinic cholinergic receptors and adrenoceptors, and SFAV neutralised many of the effects of P.volitans venom.
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The apoptogenic toxin AIP56 is a metalloprotease A-B toxin that cleaves NF-κb P65.
Daniela S Medeiros da Silva,Daniela S Medeiros da Silva,Liliana M. G. Pereira,Liliana M. G. Pereira,Ana R. Moreira,Frederico Ferreira-da-Silva,Rui M. M. Brito,Tiago Q. Faria,Irene Zornetta,Cesare Montecucco,Pedro Oliveira,Jorge E. Azevedo,Jorge E. Azevedo,Pedro Pereira,Sandra Macedo-Ribeiro,Ana do Vale,Nuno M.S. dos Santos +16 more
TL;DR: This work demonstrates that AIP56 is an A-B toxin capable of acting at distance, without requiring contact of the bacteria with the target cell, and shows that the N-terminal domain cleaves NF-κB at the Cys39-Glu40 peptide bond and that the C-terminals are involved in binding and internalization into the cytosol.
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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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•Journal Article
Mechanisms of intracellular protein transport
TL;DR: The general protein apparatus used by all eukaryotes for intracellular transport, including secretion and endocytosis, and for triggered exocyTosis of hormones and neurotransmitters, is uncovered.
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