Research Article

Structure of the Human BK Channel Ca2+-Activation Apparatus at 3.0 Å Resolution

+ See all authors and affiliations

Science  27 May 2010:
1190414
DOI: 10.1126/science.1190414

Abstract

High conductance voltage- and Ca2+-activated K+ (BK) channels encode negative feedback regulation of membrane voltage and Ca2+ signaling to play a central role in numerous physiological processes. We determined the x-ray structure of the human BK Ca2+ gating apparatus at 3.0 Å resolution and deduced its tetrameric assembly by solving a 6 Å resolution structure of a Na+-activated homolog. Two tandem C-terminal RCK domains from each of four channel subunits form a 350 kD gating ring at the intracellular membrane surface. A sequence of aspartic amino acids known as the Ca2+ bowl, located within the second of the tandem RCK domains, creates four Ca2+ binding sites on the outer perimeter of the gating ring at the “assembly interface” between RCK domains. Functionally important mutations cluster near the Ca2+ bowl, near the “flexible interface” between RCK domains, and on the surface of the gating ring facing the voltage sensors. The structure suggests that the Ca2+ gating ring, in addition to regulating the pore directly, may also modulate the voltage sensor.