Overview
- Robinson, S.D. et al. (2023) Nat Commun., 14, 2977.
Soluble in DMSO. Prepare a concentrated stock solution by dissolving the lyophilized peptide in DMSO first (e.g., at a concentration between 100-1000x of the final working concentration). Once the peptide is completely dissolved in DMSO, slowly dilute the solution into the working buffer (or water) to the desired final working concentration.
Centrifuge all product preparations before use. It is recommended to keep the DMSO concentration as low as possible. For cell assays, a final concentration of 0.1%–0.5% DMSO (v/v) is considered safe. For other experiments, a 5% DMSO (v/v) concentration is recommended.
- Alomone Labs Poneratoxin modulates NaV1.7 channel currents in stably transfected HEK293 cells.A. Representative time course, showing the effect of 3 µM (green) Poneratoxin (#STP-360) on the normalized area of NaV1.7. NaV1.7 currents were elicited by a 10 ms voltage step from the holding potential of -90 mV to -20 mV, applied every 5 sec, using whole-cell voltage clamp technique.
B. Superimposed traces of NaV1.7 current after application of control (black) and of 3 μM Poneratoxin (green), taken from the recording in A.
- Piek, T. et al. B. (1991) Comp. Biochem. Physiol. Part C: Comp. Pharmacol., 99, 481.
- Duval, A. et al. (1992) Pflugers Arch., 20, 239.
- Robinson, S.D. et al. (2023) Nat Commun., 14, 2977.
- Robinson S. D. et al. (2024) J. Biol. Chem., 300, 105577.
Delta-paraponeritoxin-Pc1a (Poneratoxin), originally isolated from the venom of Paraponera clavata (bullet ant), is a 25-amino acid peptide toxin that modulates voltage-gated sodium (Nav) channels, particularly the Nav1.6 and Nav1.7 subtypes1,2. The toxin modulates sodium channels by reducing their voltage threshold for activation and inhibiting channel inactivation with EC50 values of 97 ± 10 nM for Nav1.6 and 2.3 ± 0.4 µM for Nav1.72,3.
Structurally, Poneratoxin, along with other ant venom peptides such as Myrmicitoxin1-Pm1a, Myrmicitoxin1-Pm2a, Ectatotoxin-Rm4a and Delta-myrmicitoxin-Ta3a, represents a distinct class of Nav channel modulators. These peptides are structurally and functionally unrelated to previously described classes of peptidic Nav modulators. Their effects on Nav channel currents more closely resemble those of the “site 2” alkaloid toxins, such as batrachotoxin3,4.
Poneratoxin induces immediate, long-lasting nocifensive behaviors in mice, consistent with its potent modulation of sensory neuron Nav channels. Its activity on Nav1.7, channels expressed predominantly in peripheral sensory neurons, highlights its relevance in pain research and sodium channelopathies3.
Poneratoxin (#STP-360) is a highly pure, synthetic, and biologically active peptide toxin.