M. Schwanstecher et al., POTASSIUM CHANNEL OPENERS REQUIRE ATP TO BIND TO AND ACT THROUGH SULFONYLUREA RECEPTORS, EMBO journal (Print), 17(19), 1998, pp. 5529-5535
K-ATP channels are composed of a small inwardly rectifying K+ channel
subunit, either K(IR)6.1 or K(IR)6.2, plus a sulfonylurea receptor, SU
R1 or SUR2 (A or B), which belong to the ATP-binding cassette superfam
ily. SUR1/K(IR)6.2 reconstitute the neuronal/pancreatic beta-cell chan
nel, whereas SUR2A/K(IR)6.2 and SUR2B/K(IR)6.1 (or K(IR)6.2) are propo
sed to reconstitute the cardiac and the vascular-smooth-muscle-type K-
ATP channels, respectively. We report that potassium channel openers (
KCOs) bind to and act through SURs and that binding to SUR1, SUP2A and
SUR2B requires ATP, Non-hydrolysable ATP-analogues do not support bin
ding, and Mg2+ or Mn2+ are required. Point mutations in the Walker A m
otifs or linker regions of both nucleotide-binding folds (NBFs) abolis
h or weaken [H-3]P1075 binding to SUR2B, rendering reconstituted SUR2B
/K(IR)6.2 channels insensitive towards KCOs, The C-terminus of SUR aff
ects KCO affinity with SUR2B similar to SUR1 > SUR2A. KCOs belonging t
o different structural classes inhibited specific [H-3]P1075 binding t
o SUR2B in a monophasic manner, with the exception of minoxidil sulfat
e, which induced a biphasic displacement. The affinities of KCO bindin
g to SUR2B were 3.5-8-fold higher than their potencies for activation
of SUR2B/K(IR)6.2 channels. The results establish that SURs are the KC
O receptors of KATP channels and suggest that KCO binding requires a c
onformational change induced by ATP hydrolysis in both NBFs.