AI Article Synopsis

  • Potassium channels play a crucial role in various physiological processes, including maintaining resting membrane potential, regulating cardiac and neuronal activity, and facilitating neurotransmitter release.
  • The venom from the Tityus stigmurus scorpion can cause severe symptoms in humans and contains peptides that block potassium channels, particularly from the α-KTx and β-KTx subfamilies, with the latter being less characterized.
  • Research on T. stigmurus has identified a new β-KTx peptide, TstKMK, which is linked to the scorpion's toxins, and its 3D structure has been modeled to understand how it interacts with potassium channels, particularly through docking simulations with a specific rat potassium channel.

Article Abstract

Potassium channels are involved in the maintenance of resting membrane potential, control of cardiac and neuronal excitability, neurotransmitters release, muscle contractility and hormone secretion. The Tityus stigmurus scorpion is widely distributed in Northeastern Brazil and known to cause severe human envenomations, inducing pain, hypoesthesia, edema, erythema, paresthesia, headaches and vomiting. Most potassium channel blocking peptides that have been purified from scorpion venoms contain 30-40 amino acids with three or four disulfide bridges. These peptides belong to α-KTx subfamily. On the other hand, the β-KTx subfamily is poorly characterized, though it is very representative in some scorpion venoms. A transcriptomic approach of T.stigmurus scorpions developed by our group revealed the repertoire of possible molecules present in the venom, including many toxins of the β-KTx subfamily. One of the ESTs found, named TSTI0003C has a cDNA sequence of 538 bp codifying a mature protein with 47 amino acid residues, corresponding to 5299 Da. This β-KTx peptide is a new member of the BmTXKβ-related toxins, and was here named TstKMK. The three-dimensional structure of this potassium channel toxin of the T. stigmurus scorpion was obtained by computational modeling and refined by molecular dynamic simulations. Furthermore, we have made docking simulations using a Shaker kV-1.2 potassium channel from rats as receptor model and proposed which amino acid residues and interactions could be involved in its blockade.

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http://dx.doi.org/10.1016/j.bbrc.2012.11.044DOI Listing

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