Kir6.2-dependent high-affinity repaglinide binding to beta-cell K(ATP) channels.
1. The beta-cell K(ATP) channel is composed of two types of subunit - the inward rectifier K(+) channel (Kir6.2) which forms the channel pore, and the sulphonylurea receptor (SUR1), which serves as a regulatory subunit. The N-terminus of Kir6.2 is involved in transduction of sulphonylurea binding in...
Hlavní autoři: | Hansen, A, Hansen, J, Carr, R, Ashcroft, F, Wahl, P |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2005
|
Podobné jednotky
-
Functional coupling between Kir6.2 and SUR1 is prerequisite for [H-3]repaglinide, but not [H-3]glibenclamide, binding to pancreatic ATP-sensitive potassium (K-ATP) channels.
Autor: Hansen, A, a další
Vydáno: (2003) -
A novel SUR1/Kir6.2 specific K-ATP channel opener
Autor: Dabrowski, M, a další
Vydáno: (2001) -
Screening for mutations in the Kir6.2 subunit of the beta-cell K-ATP channel
Autor: Sakura, H, a další
Vydáno: (1996) -
Time-dependent activation of Kir6.2/SUR2A channels but not Kir6.2/SUR1 channels in the presence of ATP
Autor: Ashcroft, F, a další
Vydáno: (2001) -
Glimepiride block of Kir6.2/SUR1 Kir6.2/SUR2A and Kir6.2/SUR2A and Kir6.2/SUR2B K-ATP channels.
Autor: Ashcroft, F, a další
Vydáno: (2001)