High conductance, Ca2+-activated (BK-type) K+ channels from mouse (mSl
o) and Drosophila (dSlo) differ in their functional properties but sha
re a conserved core resembling voltage-gated K+ channels and a tail ap
pended to the core by a nonconserved linker. We have found that the ch
annel subunit is physically divisible into these two conserved domains
and that the core determines such properties as channel open time, co
nductance, and, probably, voltage dependence, whereas the tail determi
nes apparent Ca2+ sensitivity. Both domains are required for function.
We demonstrated the different roles of the core and tail by taking ad
vantage of the functional differences between mSlo and dSlo. Heterolog
ous pairing of cores and tails from mSlo and dSlo showed that single-c
hannel properties were always characteristic of the core species, but
that apparent Ca2+ sensitivity was adjusted up or down depending on th
e species of the tail. Thus, the tail is implicated in the Ca2+ sensin
g role of BK channels.