Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2066628 | Toxicon | 2008 | 7 Pages |
Abstract
The first Kv1.3 channel-selective toxin from the venom of the Iranian scorpion Odonthobuthus doriae (OdK2) was purified, sequenced and characterized physiologically.OdK2 consists of 38 amino acids, including six conserved cysteine and a C-terminal lysine residue, as revealed by the unique use of a quadrupole ion cyclotron resonance Fourier-transform mass spectrometer. Based on multiple sequence alignments, OdK2 was classified as α-KTX3.11. The pharmacological effects of OdK2 were studied on a panel of eight different cloned K+ channels (vertebrate Kv1.1–Kv1.6, Shaker IR and hERG) expressed in Xenopus laevis oocytes. Interestingly, OdK2 selectively inhibits the currents through Kv1.3 channels with an IC50 value of 7.2±2.7 nM.
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Authors
Yousra Abdel-Mottaleb, Thomas Vandendriessche, Elke Clynen, Bart Landuyt, Amir Jalali, Hossein Vatanpour, Liliane Schoofs, Jan Tytgat,