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
Snake Venoms and Other Toxic Components Affecting Thrombosis and Hemostasis
Yasuo Yamazaki,Takashi Morita +1 more
- 01 Jan 2008
TL;DR: This chapter provides an overview of the structures and functions of snake venom toxins, salivary proteins of hematophagous organisms, and also some bacteria-derived proteins that affect blood coagulation and platelet aggregation.
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Fusion of Golgi-derived vesicles mediated by SNAP-25 is essential for sympathetic neuron outgrowth but relatively insensitive to botulinum neurotoxins in vitro
Gary W. Lawrence,Jiafu Wang,Mitchell F. Brin,Mitchell F. Brin,K. Roger Aoki,Larry A. Wheeler,J. Oliver Dolly +6 more
TL;DR: In compartmentalized cultures of rat superior cervical ganglion neurons, neurites depend on SNAP‐25 for extension but this is quite resistant to BoNT/A, possibly because of a low density of SV2 at growth sites that are distant from the highly susceptible regions of neurotransmitter release.
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Crystal structure of the catalytic domain of botulinum neurotoxin subtype A3
TL;DR: In this article, the crystal structure of the catalytic domain of BoNT/A3 was determined and the structure was found to be very similar to that of LC/A1, suggesting that the overall mode of SNAP-25 binding is common between these two proteins.
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The effect of caroverine and its combination with aminooxyacetic acid on survival time of mice with experimental tetanus
TL;DR: Caroverine, given alone in a dose of 1-2 mg/kg significantly prolonged the LD50 period of mice with experimental tetanus, so the obtained results can be said that its application only at this dose proved to be effective.
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The in vitro detection of botulinum neurotoxin-cleaved endogenous VAMP is epitope-dependent.
TL;DR: Using custom made anti-VAMP antibodies against epitopes either side of the cleavage sites for BoNT/B, Bo NT/D andBoNT/F, the cleaved C-terminal VAMP fragment in cortical neurons is detected and enables quantitative assessment of the potency of VAMP-cleaving neurotoxins by a gain of signal Western blot assay.
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References
SNAP receptors implicated in vesicle targeting and fusion
Thomas H. Söllner,Sidney W. Whiteheart,Michael Brunner,Hediye Erdjument-Bromage,Scott J. Geromanos,Paul Tempst,James E. Rothman +6 more
TL;DR: The existence of numerous SNARE-related proteins, each apparently specific for a single kind of vesicles or target membrane, indicates that NSF and SNAPs may be universal components of a vesicle fusion apparatus common to both constitutive and regulated fusion (including neurotransmitter release), in which the SNAREs may help to ensure vesICLE-to-target specificity.
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SNAREpins: Minimal Machinery for Membrane Fusion
Thomas Weber,Boris V. Zemelman,James A. McNew,Benedikt Westermann,Michael Gmachl,Francesco Parlati,Thomas H. Söllner,James E. Rothman +7 more
TL;DR: Recombinant v- and t- SNARE proteins reconstituted into separate lipid bilayer vesicles assemble into SNAREpins-SNARE complexes linking two membranes, leading to spontaneous fusion of the docked membranes at physiological temperature.
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Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution
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.
TL;DR: In this article, the authors uncovered the general protein apparatus used by all eukaryotes for intracellular transport, including secretion and endocytosis, and for triggered exocytotic of hormones and neurotransmitters.
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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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