Mechanisms of inward-rectifier K+ channel inhibition by tertiapin-Q

Tertiapin-Q (TPNQ) is a derivative of honey bee toxin tertiapin (TPN) whose methionine residue is replaced with a glutamine residue. TPNQ inhibits the ROMK1 and GIRK1/4 inward-rectifier K+ channels with affinities very simila r to TPN. However, unlike native TPN, TPNQ is nonoxidizable by air. The sta bility of TPNQ allows us to investigate how it interacts with the targeted channels. We found that the interaction between TPNQ and the ROMK1 channel is a bimolecular reaction, i.e., one TPNQ molecule binds to one channel. Th e interaction surface in TPNQ is primarily formed by its alpha helix rather than the beta sheets with which scorpion toxins form their interaction sur face. The mutagenesis studies on both the channel and TPNQ together strongl y suggest that to block the K+ pore TPNQ plugs its alpha helix into the ves tibule of the K+ pore, while leaving the extended structural portion sticki ng out of the Vestibule into the extracellular media.