The relationship of brevetoxin 'length' and A-ring functionality to binding and activity in neuronal sodium channels

Authors

Robert E. Gawley, University of Miami
K Rein, University of Miami
G Jeglitsch, University of Miami
David J. Adams, University of MiamiFollow
Emmanuel A. Theodorakis, University of California, San Diego
Jorg Tiebes, University of California, San Diego
K. C Nicolaou, University of California, San Diego
D G. Baden, University of Miami

RIS ID

106143

Publication Details

Gawley, R. E., Rein, K. S., Jeglitsch, G., Adams, D. J., Theodorakis, E. A., Tiebes, J., Nicolaou, K. & Baden, D. G. (1995). The relationship of brevetoxin 'length' and A-ring functionality to binding and activity in neuronal sodium channels. Chemistry and Biology, 2 (8), 533-541.

Abstract

Background: Brevetoxins are polyether ladder toxins that are ichthyotoxic at nanomolar concentrations. They bind to voltage-gated sodium channels, causing four distinct electrophysiological effects: (i) a shift of activation potential; (ii) occurrence of subconductance states; (iii) induction of longer mean open times of the channel; and (iv) inhibition of channel inactivation. We set out to determine whether these functions all require the same structural elements within the brevetoxin molecules. Results: Several synthetically prepared structural analogs of brevetoxin B were examined in synaptosome receptor binding assays and by functional electrophysiological measurements. A truncated analog is not ichthyotoxic at micromolar concentrations, shows decreased receptor-binding affinity, and causes only a shift of activation potential without affecting mean open times or channel inactivation. An analog with the A-ring carbonyl removed binds to the receptor with nanomolar affinity, produces a shift of activation potential and inhibits inactivation, but does not induce longer mean open times. An analog in which the A-ring diol is reduced shows low binding affinity, yet populates five subconductance states. Conclusions: Our data are consistent with the hypothesis that binding to sodium channels requires an elongated cigar-shaped molecule, ∼30 Å long. The four electrophysiological effects of the brevetoxins are not produced by a single structural feature, however, since they can be decoupled by using modified ligands, which are shown here to be partial sodium channel agonists. We propose a detailed model for the binding of brevetoxins to the channel which explains the differences in the effects of the brevetoxin analogs. These studies also offer the potential for developing brevetoxin antagonists.