6Q6C | pdb_00006q6c

Pore-modulating toxins exploit inherent slow inactivation to block K+channels.

(2019) Proc Natl Acad Sci U S A 116: 18700-18709

• PubMed: 31444298 Search on PubMedSearch on PubMed Central
• DOI: https://doi.org/10.1073/pnas.1908903116
• Primary Citation of Related Structures:  
  6Q61, 6Q6C


• PubMed Abstract: 
  

  Voltage-dependent potassium channels (K _v s) gate in response to changes in electrical membrane potential by coupling a voltage-sensing module with a K ⁺ -selective pore. Animal toxins targeting K _v s are classified as pore blockers, which physically plug the ion conduction pathway, or as gating modifiers, which disrupt voltage sensor movements. A third group of toxins blocks K ⁺ conduction by an unknown mechanism via binding to the channel turrets. Here, we show that Conkunitzin-S1 (Cs1), a peptide toxin isolated from cone snail venom, binds at the turrets of K _v 1.2 and targets a network of hydrogen bonds that govern water access to the peripheral cavities that surround the central pore. The resulting ectopic water flow triggers an asymmetric collapse of the pore by a process resembling that of inherent slow inactivation. Pore modulation by animal toxins exposes the peripheral cavity of K ⁺ channels as a novel pharmacological target and provides a rational framework for drug design.

   View More

---

Organizational Affiliation: 

Department of Biomolecular Sciences, Weizmann Institute of Science, 76100 Rehovot, Israel.