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
High sensitivity of mouse neuronal cells to tetanus toxin requires a GPI-anchored protein.
Patrick Munro,Hiroshi Kojima,Jean-Luc Dupont,Jean-Louis Bossu,Bernard Poulain,Patrice Boquet +5 more
TL;DR: It is demonstrated that high sensitivity of neurons to TeNT requires rafts and one or more GPI-anchored protein which act(s) as a pivotal receptor for the neurotoxin.
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A Signaling Mechanism Coupling Netrin-1/Deleted in Colorectal Cancer Chemoattraction to SNARE-Mediated Exocytosis in Axonal Growth Cones
Tiziana Cotrufo,Francesc Pérez-Brangulí,Ashraf Muhaisen,Oriol Ros,Rosa Andrés,Thomas Baeriswyl,Giulia Fuschini,Teresa Tarragó,Marta Pascual,Jesús M. Ureña,Joan Blasi,Ernest Giralt,Esther T. Stoeckli,Eduardo Soriano +13 more
TL;DR: Evidence is provided of a new signaling mechanism that couples chemotropic Netrin-1/DCC axonal guidance and Sytx1/TI-VAMP SNARE proteins regulating membrane turnover and exocytosis.
66
Molecular basis for tetanus toxin coreceptor interactions.
TL;DR: A solid phase assay characterized the ganglioside binding specificity and functional properties of both carbohydrate binding pockets of TeNT and provided a model for how tetanus toxin utilizes coreceptors for high-affinity binding to neurons.
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Structural analysis of botulinum neurotoxin serotype F light chain: implications on substrate binding and inhibitor design.
TL;DR: The high-resolution structure of active BoNT/F catalytic domain in two crystal forms is reported, which shows the orientation of docking of the substrate at the active site is consistent with the experimental Bo NT/A-LC:SNAP-25 peptide model and the proposed model for BoNT /E- LC:SNap-25.
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Protection with Recombinant Clostridium botulinum C1 And D Binding Domain Subunit (Hc) Vaccines Against C and D Neurotoxins
Robert P. Webb,Theresa J. Smith,Patrick M. Wright,Vicki A. Montgomery,Michael M. Meagher,Leonard A. Smith +5 more
TL;DR: Results indicate the recombinant C1 and D Hc vaccines are not only effective in a monovalent formula but offer complete protection against both parental and C/D mosaic toxin and partial protection against D/C mosaic toxin when delivered as a bivalent vaccine.
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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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