Venom peptides have evolved to target a wide range of membrane proteins through diverse mechanisms of action and structures, providing promising therapeutic leads for diseases, including pain, epilepsy, and cancer, as well as unique probes of ion channel structure-function. In this work, a
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Venom peptides have evolved to target a wide range of membrane proteins through diverse mechanisms of action and structures, providing promising therapeutic leads for diseases, including pain, epilepsy, and cancer, as well as unique probes of ion channel structure-function. In this work, a high-throughput FLIPR window current screening assay on T-type Ca
V3.2 guided the isolation of a novel peptide named ω-Buthitoxin-Hf1a from scorpion
Hottentotta franzwerneri crude venom. At only 10 amino acid residues with one disulfide bond, it is not only the smallest venom peptide known to target T-type Ca
Vs but also the smallest structured scorpion venom peptide yet discovered. Synthetic Hf1a peptides were prepared with C-terminal amidation (Hf1a-NH
2) or a free C-terminus (Hf1a-OH). Electrophysiological characterization revealed Hf1a-NH
2 to be a concentration-dependent partial inhibitor of Ca
V3.2 (IC
50 = 1.18 μM) and Ca
V3.3 (IC
50 = 0.49 μM) depolarized currents but was ineffective at Ca
V3.1. Hf1a-OH did not show activity against any of the three T-type subtypes. Additionally, neither form showed activity against N-type Ca
V2.2 or L-type calcium channels. The three-dimensional structure of Hf1a-NH
2 was determined using NMR spectroscopy and used in docking studies to predict its binding site at Ca
V3.2 and Ca
V3.3. As both Ca
V3.2 and Ca
V3.3 have been implicated in peripheral pain signaling, the analgesic potential of Hf1a-NH
2 was explored in vivo in a mouse model of incision-induced acute post-surgical pain. Consistent with this role, Hf1a-NH
2 produced antiallodynia in both mechanical and thermal pain.
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