Sandbox 174
Alpha-BungarotoxinAlpha-Bungarotoxin
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[1] 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.
General StructureGeneral Structure
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 disulphide bonds, and long neurotoxins - which α-BGT falls under - are between 71-74 amino acids long and contain five per subunit. α-BGT contains 74 amino acids, and is one of the major components of Bungarus multicuntus venom. Chemical modifications of individual residues has shown that no single amino acid is mandatory for binding, signifying the significance of structure, rather than sequence, and the concept of multicontact interaction with the acetylcholine receptor [2]. The importance of structure in binding has been tested by Love & Stroud (1986)[1] by determining whether the homology and common mode of action of neurotoxins is facilitated by the three-dimensional structure. Using X-ray crystallography at various resolutions, neurotoxins erabutoxin and cobratoxin were compared to that of α-BGT to determine the level of three-dimensional similarity.
The overall size of the molecule is 40 x 30 x 20 Å, with two outer loops folded toward one another. α-BGT is "flat" enough to contain no hydrophobic core, but does contain a few uncharged sidechain groupings[1].
Secondary structure & Disulphide bondsSecondary structure & Disulphide bonds
Hydrogen bods present allow for an antiparallel β-sheet, which is the only secondary structure present and acts to keep the second and third loops roughly parallel[1]. The three-loop structure is preserved by four invariant disulphide bridges, which are present in all neurotoxins. The fifth disulphide bridge is located at the end of the second loop, and can be reduced without any effect on the binding affinity of the molecule, while a total loss of toxicity is demonstrated when the remaining disulphides are reduced, producing a random coil structure much different than the native conformation[1].
The comination of the multiple disulphide bonds and small amount of secondary structure is the cause for the extreme stability of neurotoxins like α-BGT, providing resistance to denaturing forces such as boiling[3] and strong acids[4]. Functionally important residues contained in the extended loops are preserved by the clustering of disulphides near one end of the α-BGT molecule. This is due to an increased amount of flexibility in these extended loops, which is possibly quite important for interaction with acetylcholine receptors.
FunctionsFunctions
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[1], classifying the molecule as a postsynaptic neurotoxin.
neuromuscular acetylcholine receptor bindingneuromuscular acetylcholine receptor binding
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α7 nicotinic acetylcholine receptor bindingα7 nicotinic acetylcholine receptor binding
Reponse to sensory stimuli and seizure genesis has been linked to nicotinic mechanisms[5], which are mediated by two major classes of receptors: Ganglionic type, and neuromuscular type, which pharmacological analysis of seizure genesis and habituation in the rat brain is thought to be mediated by the latter type [6]. α-BGT demonstrates this relationship due to its prominent binding in the CA3 region of the hippocampus [7].
ReferencesReferences
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Love, A.R. and Stroud, R.M. (1986) The Crystal Structure of α-Bungarotoxin at 2.5 Å resolution: Relation to Solution Structure and Binding to Acetylcholine Receptor. Protein Eng 1, 37-46. Cite error: Invalid
<ref>tag; name "main" defined multiple times with different content - ↑ Karlsson, E. (1979) in Lee,C Y (ed), Handbook of Experimental Pharmacology Springer-Verlag, Berlin Vol 52, pp 159-212;Low, B.W. (1979) In Lee,c Y (ed). Handbook of Experimental Pharmacology Springer-Verlag, Berlin, Vol 52, pp 213-257.
- ↑ Tu, A.T. and Hong, B.S (1971) J Biol Chem. 246, 2772-2779;Yang, C.C. Toxicon 12, 1-43.
- ↑ Chiceportiche, R. Rochat, C. Sampien, F. Lazdunski, M. (1972) Biochemistry 14, 2081-2091;Chen, Y.H. Tai, J.C. Huand, W.J. Lau, M.Z. Hung, M.C. Lai, M.D. Yang, J.T. (1982) Biochemistry 21 2592-2600
- ↑ Freedman, R. Wetmore, C. Stromberg, I. Leonard, S. Olsona, L. (1993) Alpha-Bungarotoxin Binding to Hippocampal Interneurons: lmmunocytochemical Characterization and Effects on Growth Factor Expression. Journal of Neuroscience 13:1965-1975.
- ↑ Miner L.L. Collins A.C. (1989) Strain comparison of nicotine-induced seizure sensitivity and nicotinic receptors. Pharmacol Biochem Behav 33, 469-475;Luntz-Leybman, V. Bickford, P. Freedman, R. (1992) Cholinergic gating of response to auditory stimuli in rat hippocampus. Brain Res 587, 130-l-36.
- ↑ Hunt, S.P. Schmidt, J. (1978) The electron microscopic autoradiographic localization of alpha-bungarotoxin binding sites within the central nervous system of the rat: Brain Res 142, 152-l 59;Segal, M. Dudai, Y. Amsterdam, A. (1978) Distribution of cu-bungarotoxin- binding cholinergic nicotinic receptor in rat brain. Brain Res 148, 105-l 19.
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