The molecular basis of G-protein inhibition of inward rectifier K+ currents was examined by co-expression of G-proteins and cloned Kir2 channel subunits in Xenopus oocytes. Channels encoded by Kir2.3 (HRK1/HIR/BIRK2/BIR11) were completely suppressed by co-expression with G-protein βγ subunits, whereas channels encoded by Kir2.1 (IRK1), which shares 60% amino acid identity with Kir2.3, were unaffected. Co-expression of Gαi1 and Gαq subunits also partially suppressed Kir2.3 currents, but Gαt, Gαs, and a constitutively active mutant of Gαil (Q204L) were ineffective. Gβγ and Kir2.3 subunits were co-immunoprecipitated using an anti-Kir2.3 antibody. Direct binding of G-protein βγ subunits to fusion proteins containing Kir2.3 N terminus, but not to fusion proteins containing Kir2.1 N terminus, was also demonstrated. The results are consistent with suppression of Kir2.3 currents resulting from a direct protein-protein interaction between the channel and G-protein βγ subunits. When Kir2.1 and Kir2.3 subunits were coexpressed, the G-protein inhibitory phenotype of Kir2.3 was dominant, suggesting that co-expression of Kir2.3 with other Kir subunits might give rise to novel G-protein-inhibitable inward rectifier currents.
Inhibition of an Inward Rectifier Potassium Channel (Kir2.3) by G-protein βγ Subunits*
N. Cohen,Q. Sha,E. Makhina,A. Lopatin,M. Linder,S. Snyder,C. Nichols
Published 1996 in Journal of Biological Chemistry
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1996
- Venue
Journal of Biological Chemistry
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1996-12-13
- Fields of study
Biology
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