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Volumn 301, Issue 4, 2011, Pages

Regulatory domain phosphorylation to distinguish the mechanistic basis underlying acute CFTR modulators

Author keywords

Cystic fibrosis; Potentiators; Protein kinase A; Short circuit current

Indexed keywords

AGENTS AFFECTING PROTEIN METABOLISM; CYCLIC AMP; FORSKOLIN; IVACAFTOR; TRANSMEMBRANE CONDUCTANCE REGULATOR; UCCF 152; UNCLASSIFIED DRUG; VRT 532;

EID: 80053353499     PISSN: 10400605     EISSN: 15221504     Source Type: Journal    
DOI: 10.1152/ajplung.00465.2010     Document Type: Article
Times cited : (29)

References (49)
  • 2
    • 0035141190 scopus 로고    scopus 로고
    • A common mechanism for cystic fibrosis transmembrane conductance regulator protein activation by genistein and benzimidazolone analogs
    • Al-Nakkash L, Hu S, Li M, Hwang TC. A common mechanism for cystic fibrosis transmembrane conductance regulator protein activation by genistein and benzimidazolone analogs. J Pharmacol Exp Ther 296: 464-472, 2001.
    • (2001) J Pharmacol Exp Ther , vol.296 , pp. 464-472
    • Al-Nakkash, L.1    Hu, S.2    Li, M.3    Hwang, T.C.4
  • 8
    • 23844483240 scopus 로고    scopus 로고
    • Phosphorylation of CFTR by PKA promotes binding of the regulatory domain
    • Chappe V, Irvine T, Liao J, Evagelidis A, Hanrahan JW. Phosphorylation of CFTR by PKA promotes binding of the regulatory domain. EMBO J 24: 2730-2740, 2005.
    • (2005) EMBO J , vol.24 , pp. 2730-2740
    • Chappe, V.1    Irvine, T.2    Liao, J.3    Evagelidis, A.4    Hanrahan, J.W.5
  • 9
    • 0035411110 scopus 로고    scopus 로고
    • - transport by cystic fibrosis transmembrane conductance regulator
    • - transport by cystic fibrosis transmembrane conductance regulator. JOP 2: 243-246, 2001.
    • (2001) JOP , vol.2 , pp. 243-246
    • Choi, J.Y.1    Lee, M.G.2    Ko, S.3    Muallem, S.4
  • 10
    • 33750499982 scopus 로고    scopus 로고
    • Thermodynamics of CFTR channel gating: A spreading conformational change initiates an irreversible gating cycle
    • Csanady L, Nairn AC, Gadsby DC. Thermodynamics of CFTR channel gating: a spreading conformational change initiates an irreversible gating cycle. J Gen Physiol 128: 523-533, 2006.
    • (2006) J Gen Physiol , vol.128 , pp. 523-533
    • Csanady, L.1    Nairn, A.C.2    Gadsby, D.C.3
  • 12
    • 0034306450 scopus 로고    scopus 로고
    • Specificity and mechanism of action of some commonly used protein kinase inhibitors
    • Davies SP, Reddy H, Caivano M, Cohen P. Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J 351: 95-105, 2000.
    • (2000) Biochem J , vol.351 , pp. 95-105
    • Davies, S.P.1    Reddy, H.2    Caivano, M.3    Cohen, P.4
  • 13
    • 0033864526 scopus 로고    scopus 로고
    • Pharmacological modulation of ion transport across wild-type and DeltaF508 CFTR-expressing human bronchial epithelia
    • Devor DC, Bridges RJ, Pilewski JM. Pharmacological modulation of ion transport across wild-type and DeltaF508 CFTR-expressing human bronchial epithelia. Am J Physiol Cell Physiol 279: C461-C479, 2000.
    • (2000) Am J Physiol Cell Physiol , vol.279
    • Devor, D.C.1    Bridges, R.J.2    Pilewski, J.M.3
  • 14
    • 3042750795 scopus 로고    scopus 로고
    • Distinct mechanisms determine the patterns of differential activation of H-Ras, N-Ras, K-Ras 4B, and M-Ras by receptors for growth factors or antigen
    • Ehrhardt A, David MD, Ehrhardt GR, Schrader JW. Distinct mechanisms determine the patterns of differential activation of H-Ras, N-Ras, K-Ras 4B, and M-Ras by receptors for growth factors or antigen. Mol Cell Biol 24: 6311-6323, 2004.
    • (2004) Mol Cell Biol , vol.24 , pp. 6311-6323
    • Ehrhardt, A.1    David, M.D.2    Ehrhardt, G.R.3    Schrader, J.W.4
  • 15
    • 32444436992 scopus 로고    scopus 로고
    • Towards an in vitro model of cystic fibrosis small airway epithelium: Characterisation of the human bronchial epithelial cell line CFBE41o
    • Ehrhardt C, Collnot EM, Baldes C, Becker U, Laue M, Kim KJ, Lehr CM. Towards an in vitro model of cystic fibrosis small airway epithelium: characterisation of the human bronchial epithelial cell line CFBE41o. Cell Tissue Res 323: 405-415, 2006.
    • (2006) Cell Tissue Res , vol.323 , pp. 405-415
    • Ehrhardt, C.1    Collnot, E.M.2    Baldes, C.3    Becker, U.4    Laue, M.5    Kim, K.J.6    Lehr, C.M.7
  • 16
    • 33645307384 scopus 로고    scopus 로고
    • The ABC protein turned chloride channel whose failure causes cystic fibrosis
    • Gadsby DC, Vergani P, Csanady L. The ABC protein turned chloride channel whose failure causes cystic fibrosis. Nature 440: 477-483, 2006.
    • (2006) Nature , vol.440 , pp. 477-483
    • Gadsby, D.C.1    Vergani, P.2    Csanady, L.3
  • 17
    • 0035200620 scopus 로고    scopus 로고
    • Cell-based assay for highthroughput quantitative screening of CFTR chloride transport agonists
    • Galietta LV, Jayaraman S, Verkman AS. Cell-based assay for highthroughput quantitative screening of CFTR chloride transport agonists. Am J Physiol Cell Physiol 281: C1734-C1742, 2001.
    • (2001) Am J Physiol Cell Physiol , vol.281
    • Galietta, L.V.1    Jayaraman, S.2    Verkman, A.S.3
  • 18
    • 1542314828 scopus 로고    scopus 로고
    • Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain
    • Howell LD, Borchardt R, Kole J, Kaz AM, Randak C, Cohn JA. Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain. Biochem J 378: 151-159, 2004.
    • (2004) Biochem J , vol.378 , pp. 151-159
    • Howell, L.D.1    Borchardt, R.2    Kole, J.3    Kaz, A.M.4    Randak, C.5    Cohn, J.A.6
  • 21
    • 0030836234 scopus 로고    scopus 로고
    • Function of the R domain in the cystic fibrosis transmembrane conductance regulator chloride channel
    • Ma J, Zhao J, Drumm ML, Xie J, Davis PB. Function of the R domain in the cystic fibrosis transmembrane conductance regulator chloride channel. J Biol Chem 272: 28133-28141, 1997.
    • (1997) J Biol Chem , vol.272 , pp. 28133-28141
    • Ma, J.1    Zhao, J.2    Drumm, M.L.3    Xie, J.4    Davis, P.B.5
  • 22
    • 33750222000 scopus 로고    scopus 로고
    • In vivo phosphorylation of CFTR promotes formation of a nucleotidebinding domain heterodimer
    • Mense M, Vergani P, White DM, Altberg G, Nairn AC, Gadsby DC. In vivo phosphorylation of CFTR promotes formation of a nucleotidebinding domain heterodimer. EMBO J 25: 4728-4739, 2006.
    • (2006) EMBO J , vol.25 , pp. 4728-4739
    • Mense, M.1    Vergani, P.2    White, D.M.3    Altberg, G.4    Nairn, A.C.5    Gadsby, D.C.6
  • 23
    • 59849091513 scopus 로고    scopus 로고
    • Direct interaction of a small-molecule modulator with G551D-CFTR, a cystic fibrosis-causing mutation associated with severe disease
    • Pasyk S, Li C, Ramjeesingh M, Bear CE. Direct interaction of a small-molecule modulator with G551D-CFTR, a cystic fibrosis-causing mutation associated with severe disease. Biochem J 418: 185-190, 2009.
    • (2009) Biochem J , vol.418 , pp. 185-190
    • Pasyk, S.1    Li, C.2    Ramjeesingh, M.3    Bear, C.E.4
  • 24
    • 24644464284 scopus 로고    scopus 로고
    • Small-molecule correctors of defective DeltaF508- CFTR cellular processing identified by high-throughput screening
    • Pedemonte N, Lukacs GL, Du K, Caci E, Zegarra-Moran O, Galietta LJ, Verkman AS. Small-molecule correctors of defective DeltaF508- CFTR cellular processing identified by high-throughput screening. J Clin Invest 115: 2564-2571, 2005.
    • (2005) J Clin Invest , vol.115 , pp. 2564-2571
    • Pedemonte, N.1    Lukacs, G.L.2    Du, K.3    Caci, E.4    Zegarra-Moran, O.5    Galietta, L.J.6    Verkman, A.S.7
  • 26
    • 78149309127 scopus 로고    scopus 로고
    • Activation of the cystic fibrosis transmembrane conductance regulator by the flavonoid quercetin: Potential use as a biomarker of DeltaF508 cystic fibrosis transmembrane conductance regulator rescue
    • Pyle LC, Fulton JC, Sloane PA, Backer K, Mazur M, Prasain J, Barnes S, Clancy JP, Rowe SM. Activation of the cystic fibrosis transmembrane conductance regulator by the flavonoid quercetin: potential use as a biomarker of DeltaF508 cystic fibrosis transmembrane conductance regulator rescue. Am J Respir Cell Mol Biol 43: 607-616, 2009.
    • (2009) Am J Respir Cell Mol Biol , vol.43 , pp. 607-616
    • Pyle, L.C.1    Fulton, J.C.2    Sloane, P.A.3    Backer, K.4    Mazur, M.5    Prasain, J.6    Barnes, S.7    Clancy, J.P.8    Rowe, S.M.9
  • 27
    • 0024424270 scopus 로고
    • Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
    • [published erratum appears in Science 1989 Sep 29, 245(4925):1437]
    • Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA [published erratum appears in Science 1989 Sep 29, 245(4925):1437]. Science 245: 1066-1073, 1989.
    • (1989) Science , vol.245 , pp. 1066-1073
    • Riordan, J.R.1    Rommens, J.M.2    Kerem, B.3    Alon, N.4    Rozmahel, R.5    Grzelczak, Z.6    Zielenski, J.7    Lok, S.8    Plavsic, N.9    Chou, J.L.10
  • 31
    • 0037971989 scopus 로고    scopus 로고
    • Kurth MJ. 3-(2- Benzyloxyphenyl)isoxazoles and isoxazolines: Synthesis and evaluation as CFTR activators
    • Sammelson RE, Ma T, Galietta LJ, Verkman AS, Kurth MJ. 3-(2- Benzyloxyphenyl)isoxazoles and isoxazolines: synthesis and evaluation as CFTR activators. Bioorg Med Chem Lett 13: 2509-2512, 2003.
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 2509-2512
    • Sammelson, R.E.1    Ma, T.2    Galietta, L.J.3    Verkman, A.S.4
  • 35
    • 42149120706 scopus 로고    scopus 로고
    • Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function
    • Serohijos AW, Hegedus T, Aleksandrov AA, He L, Cui L, Dokholyan NV, Riordan JR. Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function. Proc Natl Acad Sci USA 105: 3256-3261, 2008.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 3256-3261
    • Serohijos, A.W.1    Hegedus, T.2    Aleksandrov, A.A.3    He, L.4    Cui, L.5    Dokholyan, N.V.6    Riordan, J.R.7
  • 37
    • 29244437861 scopus 로고    scopus 로고
    • The cystic fibrosis transmembrane conductance regulator is regulated by a direct interaction with the protein phosphatase 2A
    • Thelin WR, Kesimer M, Tarran R, Kreda SM, Grubb BR, Sheehan JK, Stutts MJ, Milgram SL. The cystic fibrosis transmembrane conductance regulator is regulated by a direct interaction with the protein phosphatase 2A. J Biol Chem 280: 41512-41520, 2005.
    • (2005) J Biol Chem , vol.280 , pp. 41512-41520
    • Thelin, W.R.1    Kesimer, M.2    Tarran, R.3    Kreda, S.M.4    Grubb, B.R.5    Sheehan, J.K.6    Stutts, M.J.7    Milgram, S.L.8
  • 40
    • 20444379255 scopus 로고    scopus 로고
    • Interaction of the protein phosphatase 2A with the regulatory domain of the cystic fibrosis transmembrane conductance regulator channel
    • Vastiau A, Cao L, Jaspers M, Owsianik G, Janssens V, Cuppens H, Goris J, Nilius B, Cassiman JJ. Interaction of the protein phosphatase 2A with the regulatory domain of the cystic fibrosis transmembrane conductance regulator channel. FEBS Lett 579: 3392-3396, 2005.
    • (2005) FEBS Lett , vol.579 , pp. 3392-3396
    • Vastiau, A.1    Cao, L.2    Jaspers, M.3    Owsianik, G.4    Janssens, V.5    Cuppens, H.6    Goris, J.7    Nilius, B.8    Cassiman, J.J.9
  • 41
    • 0034192547 scopus 로고    scopus 로고
    • Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels
    • Wang F, Zeltwanger S, Hu S, Hwang TC. Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels. J Physiol 524: 637-648, 2000.
    • (2000) J Physiol , vol.524 , pp. 637-648
    • Wang, F.1    Zeltwanger, S.2    Hu, S.3    Hwang, T.C.4
  • 42
    • 0031881489 scopus 로고    scopus 로고
    • Actions of genistein on cystic fibrosis transmembrane conductance regulator channel gating. Evidence for two binding sites with opposite effects
    • Wang F, Zeltwanger S, Yang IC, Nairn AC, Hwang TC. Actions of genistein on cystic fibrosis transmembrane conductance regulator channel gating. Evidence for two binding sites with opposite effects. J Gen Physiol 111: 477-490, 1998.
    • (1998) J Gen Physiol , vol.111 , pp. 477-490
    • Wang, F.1    Zeltwanger, S.2    Yang, I.C.3    Nairn, A.C.4    Hwang, T.C.5
  • 43
    • 33745282127 scopus 로고    scopus 로고
    • Specific rescue of cystic fibrosis transmembrane conductance regulator processing mutants using pharmacological chaperones
    • Wang Y, Bartlett MC, Loo TW, Clarke DM. Specific rescue of cystic fibrosis transmembrane conductance regulator processing mutants using pharmacological chaperones. Mol Pharmacol 70: 297-302, 2006.
    • (2006) Mol Pharmacol , vol.70 , pp. 297-302
    • Wang, Y.1    Bartlett, M.C.2    Loo, T.W.3    Clarke, D.M.4
  • 44
    • 36348989763 scopus 로고    scopus 로고
    • Correctors promote maturation of cystic fibrosis transmembrane conductance regulator (CFTR)-processing mutants by binding to the protein
    • Wang Y, Loo TW, Bartlett MC, Clarke DM. Correctors promote maturation of cystic fibrosis transmembrane conductance regulator (CFTR)-processing mutants by binding to the protein. J Biol Chem 282: 33247-33251, 2007.
    • (2007) J Biol Chem , vol.282 , pp. 33247-33251
    • Wang, Y.1    Loo, T.W.2    Bartlett, M.C.3    Clarke, D.M.4
  • 45
    • 33847122608 scopus 로고    scopus 로고
    • Modulating the folding of P-glycoprotein and cystic fibrosis transmembrane conductance regulator truncation mutants with pharmacological chaperones
    • Wang Y, Loo TW, Bartlett MC, Clarke DM. Modulating the folding of P-glycoprotein and cystic fibrosis transmembrane conductance regulator truncation mutants with pharmacological chaperones. Mol Pharmacol 71: 751-758, 2007.
    • (2007) Mol Pharmacol , vol.71 , pp. 751-758
    • Wang, Y.1    Loo, T.W.2    Bartlett, M.C.3    Clarke, D.M.4
  • 46
    • 66849129301 scopus 로고    scopus 로고
    • A small-molecule modulator interacts directly with deltaPhe508-CFTR to modify its ATPase activity and conformational stability
    • Wellhauser L, Chiaw PK, Pasyk S, Li C, Ramjeesingh M, Bear CE. A small-molecule modulator interacts directly with deltaPhe508-CFTR to modify its ATPase activity and conformational stability. Mol Pharmacol 75: 1430-1438, 2009.
    • (2009) Mol Pharmacol , vol.75 , pp. 1430-1438
    • Wellhauser, L.1    Chiaw, P.K.2    Pasyk, S.3    Li, C.4    Ramjeesingh, M.5    Bear, C.E.6
  • 47
    • 0027162649 scopus 로고
    • Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
    • Welsh MJ, Smith AE. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell 73: 1251-1254, 1993.
    • (1993) Cell , vol.73 , pp. 1251-1254
    • Welsh, M.J.1    Smith, A.E.2
  • 48
    • 0030931648 scopus 로고    scopus 로고
    • Stimulation of CFTR activity by its phosphorylated R domain
    • Winter MC, Welsh MJ. Stimulation of CFTR activity by its phosphorylated R domain. Nature 389: 294-296, 1997.
    • (1997) Nature , vol.389 , pp. 294-296
    • Winter, M.C.1    Welsh, M.J.2


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