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
Transmitter uptake and release in PC12 cells overexpressing plasma membrane monoamine transporters
TL;DR: Significant modification of the secretory responses was observed, at the cell population level, upon transient expression of the serotonin transporter and of proteins known to interfere with exocytosis, such as botulinum neurotoxin C1, GTPase‐deficient Rab3 proteins, truncated Rabphilin constructs or Rim.
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Progress in rapid screening of Bacillus anthracis lethal factor activity.
Michèle Mock,Bernard P. Roques +1 more
TL;DR: Two different approaches led to the identification of the mitogen-activated protein kinases (MAPK) kinase (MKK) family of proteins as the specific substrate of LF proteolytic activity (8, 9); LF cleaves these proteins at the N terminus and thereby disrupts the transduction of extracellular signals into various biological responses including gene expression.
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Structural Insight into Exosite Binding and Discovery of Novel Exosite Inhibitors of Botulinum Neurotoxin Serotype A Through in silico Screening
TL;DR: Two recently identified exosite inhibitors are employed, D-chicoric acid and lomofungin, to probe the structural features of the exosites and molecular mechanisms of synergistic inhibition of Botulinum neurotoxin serotype A, and may provide novel candidates for structure-based development of therapeutics against BoNT/A intoxication.
Calcium-dependent acetylcholine release from Xenopus oocytes: simultaneous ionic currents and acetylcholine release recordings.
TL;DR: It is shown that SNARE proteins are present in native Xenopus oocytes and that those oocytes injected with acetylcholine and presynaptic plasma membranes extracted from the electric organ of Torpedo marmorata assume some of the functions of a cholinergic nerve terminal.
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Patent
Compositions and methods for toxigenicity testing
Regina C. M. Whitemarsh,Eric A. Johnson,Sabine Pellett,William Howard Tepp +3 more
- 28 Sep 2012
TL;DR: In this article, the use of human induced pluripotent stem (hiPS) derived cells for agent detection and analysis is discussed, and the present invention relates to compositions and methods for testing agents (e.g., Clostridium botulinum neurotoxin (BoNT) detection and analyses).
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