We have recently purified a 45 kDa protein from rat renal brush border
membrane that functions as a macromolecular nucleic acid channel when
reconstituted in artificial lipid bilayers. To explore the role of ca
lcium in the regulation of this channel, purified protein was reconsti
tuted in bilayers and calcium concentration was altered while voltage
clamp experiments were performed. Open probability of the channel was
less than 1% in 0 calcium and increased an average of 19-fold when cal
cium concentration was increased from 0 mM to 0.5 mM and 100-fold when
increased to 1.0 mM. Equimolar calcium and EDTA resulted in a fall in
open probability to 1%. Increasing calcium concentration had no effec
t on current/voltage relationship or mean open time of the channel, bu
t decreased the mean closed time significantly. Cooperative channel ga
ting was observed at 1.0 mM. These data demonstrate that open probabil
ity of the renal nucleic acid channel is calcium-dependent. The increa
se in open probability is due to an increase in channel gating activit
y rather due to an increase in the duration of the open state.