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| =Alpha-Bungarotoxin=
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| Alpha-Bungarotoxin (α-BGT) is a nicotinic cholinergic antagonist that is found within the venom of ''Bungarus multicinctus'', a South-asian snake belonging to a group commonly known as kraits. Belonging to the Elapidae Family, which consist of cobras, kraits, tiger snakes, and mambas, the venom of ''Bungarus multicuntus'' is a complex mixture of many different molecules<ref name="main">Love, A.R (FINISH)</ref> α-BGT belongs to a family of homologous proteins that act as a neurotoxic agent in the venom of these snakes. α-BGT is known to bind irreversibly to the acetylcholine receptor found at the neuromuscular junction, causing respiratory failure, paralysis, and death, as well as play an antagonstic role in binding the α7 nicotinic acetylcholine receptor in the brain.
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| =General Structure=
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| [[Image:alpha-bungarotoxin1.PNG]]
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| A large amount of highly homologous snake neurotoxins have been sequenced (>60), and can be grouped into two major classes. Short neurotoxins are between 60-62 amino acids long, and consist of four <scene name='Sandbox_174/Disulphides/1'>Disulphide Bonds</scene>
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| ==Active sites & ==
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| =Functions=
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| Elapidae neurotoxins bind specifically and tightly (with a very high affinity) in a non-covalent manner to the nicotinic acetylcholine receptors in cholinergic synapses of their victims. This prevents normal neurotransmitter-induced channel opening, which in turn blocks postsynaptic membrane depolarization<ref name="main">Love. A.R (FINISH)</ref>.
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| ==α7 nicotinic acetylcholine receptor binding==
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| Reponse to sensory stimuli and seizure genesis has been linked to nicotinic mechanisms<ref>a-Bungarotoxin Binding to Hippocampal Interneurons:
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| lmmunocytochemical Characterization and Effects on Growth Factor
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| Expression</ref>. Second note to refd<ref>article 2 </ref>
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| Seizure genesisa nd habituation of responseto sensorys timuli have been linked to nicotinic mechanisms (Marks et al., 1989;
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| Luntz-Leybman et al., 1992). These functions are closely associated
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| with the CA3 field (Schwartzkroin, 1986; Bickford-
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| Wimer et al., 1990). Nicotinic responsesa re mediated by two
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| major classeso f receptors, ganglionic type and neuromuscular
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| type. Pharmacological analysis of both seizure genesis and habituation
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| in rat brain implicates mediation by a neuromuscular
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| type (Miner and Collins, 1989; Luntz-Leybman et al., 1992).
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| These data are supported by the prominent binding of the neuromuscular-
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| type antagonist oc-bungarotoxin (a-BT) in the CA3
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| field of the hippocampus (Hunt and Schmidt, 1978; Segal et al.,
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| 1978; Clarke et al., 1985
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| ==neuromuscular acetylcholine receptor binding==
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| =References=
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| <scene name='Sandbox_174/Newscene/1'>All residues</scene> | |
| <table style="background-color:#ffffc0" cellpadding="8" width="95%" border="0"><tr><td>Please do NOT make changes to this Sandbox until after April 23, 2010. Sandboxes 151-200 are reserved until then for use by the Chemistry 307 class at UNBC taught by Prof.[[User:Andrea Gorrell|Andrea Gorrell]].</td></tr>
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