Distinct regions that control ion selectivity and calcium-dependent activation in the bestrophin ion channel.

Abstract

Cytoplasmic calcium (Ca²⁺) activates the bestrophin anion channel, allowing chloride ions to flow down their electrochemical gradient. Mutations in bestrophin 1 (BEST1) cause macular degenerative disorders. Previously, we determined an X-ray structure of chicken BEST1 that revealed the architecture of the channel. Here, we present electrophysiological studies of purified wild-type and mutant BEST1 channels and an X-ray structure of a Ca²⁺-independent mutant. From these experiments, we identify regions of BEST1 responsible for Ca²⁺ activation and ion selectivity. A "Ca²⁺ clasp" within the channel's intracellular region acts as a sensor of cytoplasmic Ca²⁺. Alanine substitutions within a hydrophobic "neck" of the pore, which widen it, cause the channel to be constitutively active, irrespective of Ca²⁺. We conclude that the primary function of the neck is as a "gate" that controls chloride permeation in a Ca²⁺-dependent manner. In contrast to what others have proposed, we find that the neck is not a major contributor to the channel's ion selectivity. We find that mutation of a cytosolic "aperture" of the pore does not perturb the Ca²⁺ dependence of the channel or its preference for anions over cations, but its mutation dramatically alters relative permeabilities among anions. The data suggest that the aperture functions as a size-selective filter that permits the passage of small entities such as partially dehydrated chloride ions while excluding larger molecules such as amino acids. Thus, unlike ion channels that have a single "selectivity filter," in bestrophin, distinct regions of the pore govern anion-vs.-cation selectivity and the relative permeabilities among anions.