Abstract
Inactivation of voltage-gated K(+) (Kv) channels mostly occurs by fast N-type or/and slow C-type mechanisms. Here, we characterized a unique mechanism of inactivation gating comprising two inactivation states in a member of the Kv channel superfamily, Kv7.1. Removal of external Ca(2+) in wild-type Kv7.1 channels produced a large, voltage-dependent inactivation, which differed from N- or C-type mechanisms. Glu(295) and Asp(317) located, respectively, in the turret and pore entrance are involved in Ca(2+) coordination, allowing Asp(317) to form H-bonding with the pore helix Trp(304), which stabilizes the selectivity filter and prevents inactivation. Phosphatidylinositol 4,5-bisphosphate (PIP2) and Ca(2+)-calmodulin prevented Kv7.1 inactivation triggered by Ca(2+)-free external solutions, where Ser(182) at the S2-S3 linker relays the calmodulin signal from its inner boundary to the external pore to allow proper channel conduction. Thus, we revealed a unique mechanism of inactivation gating in Kv7.1, exquisitely controlled by external Ca(2+) and allosterically coupled by internal PIP2 and Ca(2+)-calmodulin.