TY - JOUR
T1 - Inhibitory interactions between two inward rectifier K+ channel subunits mediated by the transmembrane domains
AU - Tucker, Stephen J.
AU - Bond, Chris T.
AU - Herson, Paco
AU - Pessia, Mauro
AU - Adelman, John P.
PY - 1996/3/8
Y1 - 1996/3/8
N2 - Inwardly rectifying K+ channel subunits may form homomeric or heteromeric channels with distinct functional properties. Hyperpolarizing commands delivered to Xenopus oocytes expressing homomeric K(ir) 4.1 channels evoke inwardly rectifying K+ currents which activate rapidly and undergo a pronounced decay at more hyperpolarized potentials. In addition, K(ir) 4.1 subunits form heteromeric channels when coexpressed with several other inward rectifier subunits. However, coexpression of K(ir) 4.1 with K(ir) 3.4 causes an inhibition of the K(ir) 4.1 current. We have investigated this inhibitory effect and show that it is mediated by interactions between the predicted transmembrane domains of the two subunit classes. Other subunits within the K(ir) 3.0 family also exhibit this inhibitory effect which can be used to define subgroups of the inward rectifier family. Further, the mechanism of inhibition is likely due to the formation of an 'inviable complex' which becomes degraded, rather than by formation of stable nonconductive heteromeric channels. These results provide insight into the assembly and regulation of inwardly rectifying K+ channels and the domains which define their interactions.
AB - Inwardly rectifying K+ channel subunits may form homomeric or heteromeric channels with distinct functional properties. Hyperpolarizing commands delivered to Xenopus oocytes expressing homomeric K(ir) 4.1 channels evoke inwardly rectifying K+ currents which activate rapidly and undergo a pronounced decay at more hyperpolarized potentials. In addition, K(ir) 4.1 subunits form heteromeric channels when coexpressed with several other inward rectifier subunits. However, coexpression of K(ir) 4.1 with K(ir) 3.4 causes an inhibition of the K(ir) 4.1 current. We have investigated this inhibitory effect and show that it is mediated by interactions between the predicted transmembrane domains of the two subunit classes. Other subunits within the K(ir) 3.0 family also exhibit this inhibitory effect which can be used to define subgroups of the inward rectifier family. Further, the mechanism of inhibition is likely due to the formation of an 'inviable complex' which becomes degraded, rather than by formation of stable nonconductive heteromeric channels. These results provide insight into the assembly and regulation of inwardly rectifying K+ channels and the domains which define their interactions.
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U2 - 10.1074/jbc.271.10.5866
DO - 10.1074/jbc.271.10.5866
M3 - Article
C2 - 8621458
AN - SCOPUS:0029880484
SN - 0021-9258
VL - 271
SP - 5866
EP - 5870
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 10
ER -