1kfh
From Proteopedia
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[[Image:1kfh.jpg|left|200px]] | [[Image:1kfh.jpg|left|200px]] | ||
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'''Solution Structure of alpha-Bungarotoxin by NMR Spectroscopy''' | '''Solution Structure of alpha-Bungarotoxin by NMR Spectroscopy''' | ||
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[[Category: Moise, L.]] | [[Category: Moise, L.]] | ||
[[Category: Piserchio, A.]] | [[Category: Piserchio, A.]] | ||
- | [[Category: | + | [[Category: Alpha-bungarotoxin]] |
- | [[Category: | + | [[Category: Long snake neurotoxin]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 22:40:56 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 19:40, 2 May 2008
Solution Structure of alpha-Bungarotoxin by NMR Spectroscopy
Overview
We report a new, higher resolution NMR structure of alpha-bungarotoxin that defines the structure-determining disulfide core and beta-sheet regions. We further report the NMR structure of the stoichiometric complex formed between alpha-bungarotoxin and a recombinantly expressed 19-mer peptide ((178)IPGKRTESFYECCKEPYPD(196)) derived from the alpha7 subunit of the chick neuronal nicotinic acetylcholine receptor. A comparison of these two structures reveals binding-induced stabilization of the flexible tip of finger II in alpha-bungarotoxin. The conformational rearrangements in the toxin create an extensive binding surface involving both sides of the alpha7 19-mer hairpin-like structure. At the contact zone, Ala(7), Ser(9), and Ile(11) in finger I and Arg(36), Lys(38), Val(39), and Val(40) in finger II of alpha-bungarotoxin interface with Phe(186), Tyr(187), Glu(188), and Tyr(194) in the alpha7 19-mer underscoring the importance of receptor aromatic residues as critical neurotoxin-binding determinants. Superimposing the structure of the complex onto that of the acetylcholine-binding protein (1I9B), a soluble homologue of the extracellular domain of the alpha7 receptor, places alpha-bungarotoxin at the peripheral surface of the inter-subunit interface occluding the agonist-binding site. The disulfide-rich core of alpha-bungarotoxin is suggested to be tilted in the direction of the membrane surface with finger II extending into the proposed ligand-binding cavity.
About this Structure
1KFH is a Single protein structure of sequence from Bungarus multicinctus. Full crystallographic information is available from OCA.
Reference
NMR structural analysis of alpha-bungarotoxin and its complex with the principal alpha-neurotoxin-binding sequence on the alpha 7 subunit of a neuronal nicotinic acetylcholine receptor., Moise L, Piserchio A, Basus VJ, Hawrot E, J Biol Chem. 2002 Apr 5;277(14):12406-17. Epub 2002 Jan 14. PMID:11790782 Page seeded by OCA on Fri May 2 22:40:56 2008