BmTx3

BmTx3 is a

BmTx3 was originally purified from the venom of the Chinese scorpion, Buthus Martensi Karsch. BmTx3 is a “short-chain” peptide like other potassium channel blockers in the scorpion venom and added to the phylogenetic tree in the subfamily α-KTx15. Its 3D structure has not yet been elucidated, but based on sequence similarity it likely resembles the 3D structure of BmTx1 ^[1] or Discrepin.^[2]

Biochemistry

BmTx3 consists of an α-helix and two β-sheet segments cross-linked by three disulfide bridges (Cs-α/β motif).

Target

BmTx3 is the first toxin from the scorpion α-KTx subfamily 15 ^[3] with two functional faces. As all α-KTx peptides, BmTx3 blocks A-type (I_A) potassium currents (K_D = 54 nM). BmTx3 blocks primarily the Kv4.x proteins and has a higher affinity for Kv4.1 channels than for Kv4.2 and Kv4.3 channels.^[4] The second functional face of BmTx3 blocks the hERG (human Ether-à-go-go) channel (K_D = 2 μM), a characteristic belonging to γ-KTx peptides.^[4] BmTx3 binding site seems essentially localized in

The other functional face is thought to be situated at the α-helix-side and composed of Arg¹⁸ and Lys¹⁹, like the functional face of other hERG toxins. It is known that α-KTx peptides use the β-sheet side to interact with the receptor, whereas γ-KTx peptides usually use their α-helix-side.[5] As BmTx3 seems to use both sides to bind to different potassium channels, it might be an evolutionary transient between the two families.^[5]

Toxicity

When injected into mice it causes epileptiform behavior.^[6] This might be due to its effect on A-type K⁺ channels, which, like the Kv4.x, are involved in action potential back propagation, firing frequency, spike initiation and action potential waveform determination.^[4] Blocking of the hERG channel can cause drug-induced long QT syndrome, arrhythmias and ventricular fibrillation which can result in death.^[5]

References