Multiple regulatory sites in large-conductance calcium-activated potassium channels

Abstract

Large conductance, Ca²⁺- and voltage-activated K⁺ channels (BK) respond to two distinct physiological signals—membrane voltage and cytosolic Ca²⁺ (refs 1, 2). Channel opening is regulated by changes in Ca²⁺ concentration spanning 0.5 µM to 50 mM (refs 2–5), a range of Ca²⁺ sensitivity unusual among Ca²⁺-regulated proteins. Although voltage regulation arises from mechanisms shared with other voltage-gated channels^6,7,8, the mechanisms of Ca²⁺ regulation remain largely unknown. One potential Ca²⁺-regulatory site, termed the ‘Ca²⁺ bowl’, has been located to the large cytosolic carboxy terminus^9,10,11. Here we show that a second region of the C terminus, the RCK domain (regulator of conductance for K⁺ (ref. 12)), contains residues that define two additional regulatory effects of divalent cations. One site, together with the Ca²⁺ bowl, accounts for all physiological regulation of BK channels by Ca²⁺; the other site contributes to effects of millimolar divalent cations that may mediate physiological regulation by cytosolic Mg²⁺ (refs 5, 13). Independent regulation by multiple sites explains the large concentration range over which BK channels are regulated by Ca²⁺. This allows BK channels to serve a variety of physiological roles contingent on the Ca²⁺ concentration to which the channels are exposed^14,15.