Structure-function map of the receptor site for β-scorpion toxins in domain II of voltage-gated sodium channels

Joel Z. Zhang, Vladimir Yarov-Yarovoy, Todd Scheuer, Izhar Karbat, Lior Cohen, Dalia Gordon, Michael Gurevitz, William A. Catterall

Research output: Contribution to journalArticle

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Abstract

Voltage-gated sodium (Na v) channels are the molecular targets of β-scorpion toxins, which shift the voltage dependence of activation to more negative membrane potentials by a voltage sensor-trapping mechanism. Molecular determinants of β-scorpion toxin (CssIV) binding and action on rat brain sodium channels are located in the S1-S2 (IIS1-S2) and S3-S4 (IIS3-S4) extracellular linkers of the voltage-sensing module in domain II. In IIS1-S2, mutations of two amino acid residues (Glu 779 and Pro 782) significantly altered the toxin effect by reducing binding affinity. In IIS3-S4, six positions surrounding the key binding determinant, Gly 845, define a hot spot of high-impact residues. Two of these substitutions (A841N and L846A) reduced voltage sensor trapping. The other three substitutions (N842R, V843A, and E844N) increased voltage sensor trapping. These bidirectional effects suggest that the IIS3-S4 loop plays a primary role in determining both toxin affinity and efficacy. A high resolution molecular model constructed with the Rosetta-Membrane modeling system reveals interactions of amino acid residues in sodium channels that are crucial for toxin action with residues in CssIV that are required for its effects. In this model, the wedge-shaped CssIV inserts between the IIS1-S2 and IIS3-S4 loops of the voltage sensor, placing key amino acid residues in position to interact with binding partners in these extracellular loops. These results provide new molecular insights into the voltage sensor-trapping model of toxin action and further define the molecular requirements for the development of antagonists that can prevent or reverse toxicity of scorpion toxins.

Original languageEnglish (US)
Pages (from-to)33641-33651
Number of pages11
JournalJournal of Biological Chemistry
Volume286
Issue number38
DOIs
StatePublished - Sep 23 2011

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Voltage-Gated Sodium Channels
Scorpions
Sodium Channels
Amino Acids
Electric potential
Molecular Models
Sensors
Membrane Potentials
Sodium
Mutation
Substitution reactions
Membranes
Brain
scorpion toxin receptor
Toxicity
Rats
Chemical activation

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Structure-function map of the receptor site for β-scorpion toxins in domain II of voltage-gated sodium channels. / Zhang, Joel Z.; Yarov-Yarovoy, Vladimir; Scheuer, Todd; Karbat, Izhar; Cohen, Lior; Gordon, Dalia; Gurevitz, Michael; Catterall, William A.

In: Journal of Biological Chemistry, Vol. 286, No. 38, 23.09.2011, p. 33641-33651.

Research output: Contribution to journalArticle

Zhang, Joel Z. ; Yarov-Yarovoy, Vladimir ; Scheuer, Todd ; Karbat, Izhar ; Cohen, Lior ; Gordon, Dalia ; Gurevitz, Michael ; Catterall, William A. / Structure-function map of the receptor site for β-scorpion toxins in domain II of voltage-gated sodium channels. In: Journal of Biological Chemistry. 2011 ; Vol. 286, No. 38. pp. 33641-33651.
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