| Literature DB >> 24704423 |
Zongyun Chen1, Youtian Hu2, Jun Hu2, Weishan Yang2, Jean-Marc Sabatier3, Michel De Waard4, Zhijian Cao2, Wenxin Li1, Song Han5, Yingliang Wu6.
Abstract
Besides classical scorpion toxin-potassium channel binding modes, novel modes remain unknown. Here, we report a novel binding mode of native toxin BmKTX towards Kv1.3 channel. The combined experimental and computational data indicated that BmKTX-D33H analog used the classical anti-parallel β-sheet domain as the channel-interacting interface together with the conserved channel pore-blocking Lys(26). However, the wild-type BmKTX was found to use Arg(23) rather than Lys(26) as the new pore-blocking residue, and mainly adopt the turn motif between the α-helix and antiparallel β-sheet domains to recognize Kv1.3 channel. Together, these findings not only reveal that scorpion toxin-potassium channel interaction modes are more diverse than thought, but also highlight the functional role of toxin acidic residues in mediating diverse toxin-potassium channel binding modes.Entities:
Keywords: Acidic residues; Binding mode; BmKTX-D33H analog; Electrostatic repulsion; Potassium channels; Scorpion toxin BmKTX
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Year: 2014 PMID: 24704423 DOI: 10.1016/j.bbrc.2014.03.101
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575