TY - JOUR
T1 - Cloning and functional expression of the cDNA encoding an inwardly-rectifying potassium channel expressed in pancreatic β-cells and in the brain
AU - Bond, C.T.
AU - Ämmälä, C.
AU - Ashfield, R.
AU - Blair, T.A.
AU - Gribble, F.
AU - Khan, R.N.
AU - Lee, K.
AU - Proks, P.
AU - Rowe, I.C.M.
AU - Sakura, H.
AU - Ashford, M.J.
AU - Adelman, J.P.
AU - Ashcroft, F.M.
PY - 1995
Y1 - 1995
N2 - A cDNA clone encoding an inwardly-rectifying K-channel (BIR1) was isolated from insulinoma cells. The predicted amino acid sequence shares 72% identity with the cardiac ATP-sensitive K-channel rcKATP (KATP-1; [6]). The mRNA is expressed in the brain and insulinoma cells. Heterologous expression in Xenopus oocytes produced currents which were K+-selective, time-independent and showed inward rectification. The currents were blocked by external barium and caesium, but insensitive to tolbutamide and diazoxide. In inside-out patches, channel activity was not blocked by 1 mM internal ATP. The sequence homology with KATP-1 suggests that BIR1 is a subunit of a brain and β-cell KATP channel. However, pharmacological differences and the lack of ATP-sensitivity, suggest that if, this is the case, heterologous subunits must exert strong modulatory influences on the native channel.
AB - A cDNA clone encoding an inwardly-rectifying K-channel (BIR1) was isolated from insulinoma cells. The predicted amino acid sequence shares 72% identity with the cardiac ATP-sensitive K-channel rcKATP (KATP-1; [6]). The mRNA is expressed in the brain and insulinoma cells. Heterologous expression in Xenopus oocytes produced currents which were K+-selective, time-independent and showed inward rectification. The currents were blocked by external barium and caesium, but insensitive to tolbutamide and diazoxide. In inside-out patches, channel activity was not blocked by 1 mM internal ATP. The sequence homology with KATP-1 suggests that BIR1 is a subunit of a brain and β-cell KATP channel. However, pharmacological differences and the lack of ATP-sensitivity, suggest that if, this is the case, heterologous subunits must exert strong modulatory influences on the native channel.
UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-0029071861&partnerID=MN8TOARS
U2 - 10.1016/0014-5793(95)00497-W
DO - 10.1016/0014-5793(95)00497-W
M3 - Article
SN - 0014-5793
VL - 367
SP - 61
EP - 66
JO - FEBS LETTERS
JF - FEBS LETTERS
IS - 1
ER -