|
||
The Journal of General Physiology, Vol 107, 381-397, Copyright © 1996 by The Rockefeller University Press
ARTICLES |
KW Chan, MN Langan, JL Sui, JA Kozak, A Pabon, JA Ladias and DE Logothetis
Department of Physiology and Biophysics, City University of New York, New York 10029, USA.
GTP-binding (G) proteins have been shown to mediate activation of inwardly rectifying potassium (K+) channels in cardiac, neuronal and neuroendocrine cells. Here, we report functional expression of a recombinant inwardly rectifying channel which we call KGP (or hpKir3.4), to signify that it is K+ selective, G-protein-gated and isolated from human pancreas. KGP expression in Xenopus oocytes resulted in sizeable basal (or agonist-independent) currents while coexpression with a G-protein-linked receptor, yielded additional agonist-induced currents. Coexpression of KGP and hGIRK1 (a human brain homolog of GIRK1/Kir3.1) produced much larger basal currents than those observed with KGP or hGIRK1 alone, and upon coexpression with receptor, similarly large agonist-induced currents could be obtained. Pertussis toxin treatment significantly diminished agonist-dependent currents due to either KGP or KGP/hGIRK1 expression. Interestingly, PTX also significantly reduced basal KGP or KGP/hGIRK1 currents, suggesting that basal activity is largely the result of G-protein gating as well. When the two channels were coexpressed with receptor, the relative increase in current elicited by agonist was similar whether KGP and hGIRK1 were expressed alone or together. When in vitro translated or when expressed in Xenopus oocytes or CHO mammalian cells, KGP gave rise to a nonglycosylated 45-kD protein. Antibodies directed against either KGP or hGIRK1 coprecipitated both proteins coexpressed in oocytes, providing evidence for the heteromeric assembly of the two channels and suggesting that the current potentiation seen with coexpression of the two channel subunits is due to specific interactions between them. An endogenous oocyte protein similar in size to KGP was also coprecipitated with hGIRK1.
This article has been cited by other articles:
![]() |
R. Rusinova, T. Mirshahi, and D. E. Logothetis Specificity of Gbeta{gamma} Signaling to Kir3 Channels Depends on the Helical Domain of Pertussis Toxin-sensitive G{alpha} Subunits J. Biol. Chem., November 23, 2007; 282(47): 34019 - 34030. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. E. Logothetis, D. Lupyan, and A. Rosenhouse-Dantsker Diverse Kir modulators act in close proximity to residues implicated in phosphoinositide binding J. Physiol., August 1, 2007; 582(3): 953 - 965. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Humrich, C. Bermel, M. Bunemann, L. Harmark, R. Frost, U. Quitterer, and M. J. Lohse Phosducin-like Protein Regulates G-Protein {beta}{gamma} Folding by Interaction with Tailless Complex Polypeptide-1{alpha}: DEPHOSPHORYLATION OR SPLICING OF PhLP TURNS THE SWITCH TOWARD REGULATION OF G{beta}{gamma} FOLDING J. Biol. Chem., May 20, 2005; 280(20): 20042 - 20050. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. D. McAllister, D. P. Hurst, J. Barnett-Norris, D. Lynch, P. H. Reggio, and M. E. Abood Structural Mimicry in Class A G Protein-coupled Receptor Rotamer Toggle Switches: THE IMPORTANCE OF THE F3.36(201)/W6.48(357) INTERACTION IN CANNABINOID CB1 RECEPTOR ACTIVATION J. Biol. Chem., November 12, 2004; 279(46): 48024 - 48037. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kittel, J. Pelletier, F. Bigonnesse, O. Guckelberger, K. Kordas, N. Braun, S. C. Robson, and J. Sevigny Localization of Nucleoside Triphosphate Diphosphohydrolase-1 (NTPDase1) and NTPDase2 in Pancreas and Salivary Gland J. Histochem. Cytochem., July 1, 2004; 52(7): 861 - 871. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Leaney, A. Benians, S. Brown, M. Nobles, D. Kelly, and A. Tinker Rapid desensitization of G protein-gated inwardly rectifying K+ currents is determined by G protein cycle Am J Physiol Cell Physiol, July 1, 2004; 287(1): C182 - C191. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Benians, J. L. Leaney, G. Milligan, and A. Tinker The Dynamics of Formation and Action of the Ternary Complex Revealed in Living Cells Using a G-protein-gated K+ Channel as a Biosensor J. Biol. Chem., March 14, 2003; 278(12): 10851 - 10858. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Rohacs, C. M. B. Lopes, T. Jin, P. P. Ramdya, Z. Molnar, and D. E. Logothetis Specificity of activation by phosphoinositides determines lipid regulation of Kir channels PNAS, January 21, 2003; 100(2): 745 - 750. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. V. Kuzhikandathil and G. S. Oxford Classic D1 Dopamine Receptor Antagonist R-(+)-7-Chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride (SCH23390) Directly Inhibits G Protein-Coupled Inwardly Rectifying Potassium Channels Mol. Pharmacol., July 1, 2002; 62(1): 119 - 126. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Mirshahi, L. Robillard, H. Zhang, T. E. Hebert, and D. E. Logothetis Gbeta Residues That Do Not Interact with Galpha Underlie Agonist-independent Activity of K+ Channels J. Biol. Chem., February 22, 2002; 277(9): 7348 - 7355. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. He, X. Yan, H. Zhang, T. Mirshahi, T. Jin, A. Huang, and D. E. Logothetis Identification of Critical Residues Controlling G Protein-gated Inwardly Rectifying K+ Channel Activity through Interactions with the beta gamma Subunits of G Proteins J. Biol. Chem., February 15, 2002; 277(8): 6088 - 6096. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Rohacs, J. Chen, G. D. Prestwich, and D. E. Logothetis Distinct Specificities of Inwardly Rectifying K+ Channels for Phosphoinositides J. Biol. Chem., December 17, 1999; 274(51): 36065 - 36072. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. D. McAllister, G. Griffin, L. S. Satin, and M. E. Abood Cannabinoid Receptors Can Activate and Inhibit G Protein-Coupled Inwardly Rectifying Potassium Channels in a Xenopus Oocyte Expression System J. Pharmacol. Exp. Ther., November 1, 1999; 291(2): 618 - 626. [Abstract] [Full Text] |
||||
![]() |
C. He, H. Zhang, T. Mirshahi, and D. E. Logothetis Identification of a Potassium Channel Site That Interacts with G Protein beta gamma Subunits to Mediate Agonist-induced Signaling J. Biol. Chem., April 30, 1999; 274(18): 12517 - 12524. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Corey and D. E. Clapham Identification of Native Atrial G-protein-regulated Inwardly Rectifying K+ (GIRK4) Channel Homomultimers J. Biol. Chem., October 16, 1998; 273(42): 27499 - 27504. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Negulescu, L. E.-C. Leong, K. G. Chandy, B. L. Semler, and G. A. Gutman Translation Initiation of a Cardiac Voltage-gated Potassium Channel by Internal Ribosome Entry J. Biol. Chem., August 7, 1998; 273(32): 20109 - 20113. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Sui, J. Petit-Jacques, and D. E. Logothetis Activation of the atrial KACh channel by the beta gamma subunits of G proteins or intracellular Na+ ions depends on the presence of phosphatidylinositol phosphates PNAS, February 3, 1998; 95(3): 1307 - 1312. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ji, S. A. John, Y. Lu, and J. N. Weiss Mechanosensitivity of the Cardiac Muscarinic Potassium Channel. A NOVEL PROPERTY CONFERRED BY Kir3.4 SUBUNIT J. Biol. Chem., January 16, 1998; 273(3): 1324 - 1328. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Vivaudou, K. W. Chan, J.-L. Sui, L. Y. Jan, E. Reuveny, and D. E. Logothetis Probing the G-protein Regulation of GIRK1 and GIRK4, the Two Subunits of the KACh Channel, Using Functional Homomeric Mutants J. Biol. Chem., December 12, 1997; 272(50): 31553 - 31560. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Woodward, E. B. Stevens, and R. D. Murrell-Lagnado Molecular Determinants for Assembly of G-protein-activated Inwardly Rectifying K+ Channels J. Biol. Chem., April 18, 1997; 272(16): 10823 - 10830. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. W. Chan, J. L. Sui, M. Vivaudou, and D. E. Logothetis Specific Regions of Heteromeric Subunits Involved in Enhancement of G Protein-gated K+ Channel Activity J. Biol. Chem., March 7, 1997; 272(10): 6548 - 6555. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. W. Chan, J.-L. Sui, M. Vivaudou, and D. E. Logothetis Control of channel activity through a unique amino acid residue of a G protein-gated inwardly rectifying K+ channel subunit PNAS, November 26, 1996; 93(24): 14193 - 14198. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Pabon, K. W. Chan, J. L. Sui, X. Wu, D. E. Logothetis, and W. B. Thornhill Glycosylation of GIRK1 at Asn119 and ROMK1 at Asn117 Has Different Consequences in Potassium Channel Function J. Biol. Chem., September 22, 2000; 275(39): 30677 - 30682. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. J. Hill and E. G. Peralta Inhibition of a Gi-activated Potassium Channel (GIRK1/4) by the Gq-coupled m1 Muscarinic Acetylcholine Receptor J. Biol. Chem., February 16, 2001; 276(8): 5505 - 5510. [Abstract] [Full Text] [PDF] |
||||
|
|