Cobatoxin

Abstract: Potassium-channel-blocking scorpion toxins (α-K-toxins) have been shown to be valuable tools for the study of potassium channels. Here we report two toxins, cobatoxin 1 and 2, of 32 amino acids, containing three disulphide bridges, that were isolated from the venom of the Mexican scorpion Centruroides noxius. Their primary sequences show less than 40 % identity to other α-K-toxins. It is therefore proposed that they belong to subfamily 9. The cDNA of cobatoxin 1 encodes a putative signal peptide, a putative short propeptide, the mature peptide and two amino acids that are processed to leave cobatoxin 1 amidated at the C-terminus. In rat brain synaptosomal membranes cobatoxin 1 and cobatoxin 2 bind to a common binding site of α-K-toxins with Ki values of 109 pM and 87 pM, respectively. Moreover, they block the Shaker and KV1.1 K+ channels with moderate affinities, with Kd values of around 0.7 μM and 4.1 μM (Shaker) and 0.5 μM and 1.0 μM (KV1.1), respectively. A three-dimensional model of cobatoxin 1 was generated and used to interpret the obtained functional data on a structural basis.