Identification and biochemical characterization of the SLC9A7 interactome

References

• Pouyssegur J, Sardet C, Franchi A, L'Allemain G, Paris S. A specific mutation abolishing Na + /H+ antiport activity in hamster fibroblasts precludes growth at neutral and acidic pH. Proc Natl Acad Sci USA 1984; 81: 4833–4837
   PubMed Web of Science ®Google Scholar
• Orlowski J, Grinstein S. Diversity of the mammalian sodium/proton exchanger SLC9 gene family. Pflugers Arch 2004; 447: 549–565
   PubMed Web of Science ®Google Scholar
• Numata M, Orlowski J. Molecular cloning and characterization of a novel (Na+, K+)/H+ exchanger localized to the trans-Golgi network. J Biol Chem 2001; 276: 17387–17394
   PubMed Web of Science ®Google Scholar
• Bowers K, Levi BP, Patel FI, Stevens TH. The sodium/proton exchanger Nhx1p is required for endosomal protein trafficking in the yeast Saccharomyces cerevisiae. Mol Biol Cell 2000; 11: 4277–4294
   PubMed Web of Science ®Google Scholar
• Lin PJ, Williams WP, Luu Y, Molday RS, Orlowski J, Numata M. Secretory carrier membrane proteins interact and regulate trafficking of the organellar (Na+, K+)/H+ exchanger NHE7. J Cell Sci 2005; 118: 1885–1897
   PubMed Web of Science ®Google Scholar
• Lin PJ, Williams WP, Kobiljski J, Numata M. Caveolins bind to (Na+, K+)/H+ exchanger NHE7 by a novel binding module. Cell Signal 2007; 19: 978–988
   PubMed Web of Science ®Google Scholar
• de Hoog CL, Foster LJ, Mann M. RNA and RNA binding proteins participate in early stages of cell spreading through spreading initiation centers. Cell 2004; 117: 649–662
   PubMed Web of Science ®Google Scholar
• Rappsilber J, Ishihama Y, Mann M. Stop and go extraction tips for matrix-assisted laser desorption/ionization, nanoelectrospray, and LC/MS sample pretreatment in proteomics. Anal Chem 2003; 75: 663–670
   PubMed Web of Science ®Google Scholar
• Chan QW, Howes CG, Foster LJ. Quantitative comparison of caste differences in honeybee hemolymph. Mol Cell Proteomics 2006; 5: 2252–2262
   Google Scholar
• Harlow E, Lane D. 1988. Antibodies: A laboratory manual Cold Spring Harbor Laboratory.
   Google Scholar
• Jurado LA, Chockalingam PS, Jarrett HW. Apocalmodulin. Physiol Rev 1999; 79: 661–682
   PubMed Web of Science ®Google Scholar
• Wakabayashi S, Shigekawa M, Pouyssegur J. Molecular physiology of vertebrate Na+/H+ exchangers. Physiol Rev 1997; 77: 51–74
   PubMed Web of Science ®Google Scholar
• Cimler BM, Andreasen TJ, Andreasen KI, Storm DR. P-57 is a neural specific calmodulin-binding protein. J Biol Chem 1985; 260: 10784–10788
   PubMed Web of Science ®Google Scholar
• Bertrand B, Wakabayashi S, Ikeda T, Pouyssegur J, Shigekawa M. The Na+/H+ exchanger isoform 1 (NHE1) is a novel member of the calmodulin-binding proteins. Identification and characterization of calmodulin-binding sites. J Biol Chem 1994; 269: 13703–13709
   PubMed Web of Science ®Google Scholar
• Matsushima N, Hayashi N, Jinbo Y, Izumi Y. Ca2 + -bound calmodulin forms a compact globular structure on binding four trifluoperazine molecules in solution. Biochem J 2000; 347: 211–215
   Google Scholar
• Osawa M, Swindells MB, Tanikawa J, Tanaka T, Mase T, Furuya T, Ikura M. Solution structure of calmodulin-W-7 complex: The basis of diversity in molecular recognition. J Mol Biol 1998; 276: 165–176
   PubMed Web of Science ®Google Scholar
• Dalgarno DC, Klevit RE, Levine BA, Scott GM, Williams RJ, Gergely J, Grabarek Z, Leavis PC, Grand RJ, Drabikowski W. The nature of the trifluoperazine binding sites on calmodulin and troponin-C. Biochim Biophys Acta 1984; 791: 164–172
   Google Scholar
• Hidaka H, Yamaki T, Naka M, Tanaka T, Hayashi H, Kobayashi R. Calcium-regulated modulator protein interacting agents inhibit smooth muscle calcium-stimulated protein kinase and ATPase. Mol Pharmacol 1980; 17: 66–72
   PubMed Web of Science ®Google Scholar
• Massom L, Lee H, Jarrett HW. Trifluoperazine binding to porcine brain calmodulin and skeletal muscle troponin C. Biochemistry 1990; 29: 671–681
   PubMed Web of Science ®Google Scholar
• Mazzochi C, Benos DJ, Smith PR. Interaction of epithelial ion channels with the actin-based cytoskeleton. Am J Physiol Renal Physiol 2006; 291: F1113–1122
   PubMed Web of Science ®Google Scholar
• Alexander RT, Furuya W, Szaszi K, O J., Grinstein S. Rho GTPases dictate the mobility of the Na+/H+ exchanger NHE3 in epithelia: Role in apical retention and targeting. Proc Natl Acad Sci USA 2005; 102: 12253–12258
   PubMed Web of Science ®Google Scholar
• Cha B, Tse M, Yun C, Kovbasnjuk O, Mohan S, Hubbard A, Arpin M, Donowitz M. The NHE3 juxtamembrane cytoplasmic domain directly binds ezrin: Dual role in NHE3 trafficking and mobility in the brush border. Mol Biol Cell 2006; 17: 2661–2673
   PubMed Web of Science ®Google Scholar
• Szaszi K, Paulsen A, Szabo EZ, Numata M, Grinstein S, Orlowski J. Clathrin-mediated endocytosis and recycling of the neuron-specific Na+/H+ exchanger NHE5 isoform. Regulation by phosphatidylinositol 3′-kinase and the actin cytoskeleton. J Biol Chem 2002; 277: 42623–42632
   Google Scholar
• Lagana A, Vadnais J, Le PU, Nguyen TN, Laprade R, Nabi IR, Noel J. Regulation of the formation of tumor cell pseudopodia by the Na+/H+ exchanger NHE1. J Cell Sci 2000; 113: 3649–3662
   PubMed Web of Science ®Google Scholar
• Cardone RA, Casavola V, Reshkin SJ. The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis. Nat Rev Cancer 2005; 5: 786–795
   PubMed Web of Science ®Google Scholar
• Watts III BA, George T, Good DW. The basolateral NHE1 Na+/H+ exchanger regulates transepithelial HCO3- absorption through actin cytoskleton remodeling in renal thick ascending limb. J Biol Chem 2005; 280: 11439–11447
   PubMed Web of Science ®Google Scholar
• Helfand BT, Chang L, Goldman RD. Intermediate filaments are dynamic and motile elements of cellular architecture. J Cell Sci 2004; 117: 133–141
   Web of Science ®Google Scholar
• Esue O, Carson AA, Tseng Y, Wirtz D. A direct interaction between actin and vimentin filaments mediated by the tail domain of vimentin. J Biol Chem 2006; 281: 30393–30399
   PubMed Web of Science ®Google Scholar
• Schwartz MA, Lechene C, Ingber DE. Insoluble fibronectin activates the Na + /H+ antiporter by clustering and immobilizing integrin alpha 5 beta 1, independent of cell shape. Proc Natl Acad Sci USA 1991; 88: 7849–7853
   PubMed Web of Science ®Google Scholar
• Grinstein S, Woodside M, Waddell TK, Downey GP, Orlowski J, Pouyssegur J, Wong DC, Foskett JK. Focal localization of the NHE-1 isoform of the Na + /H+ antiport: Assessment of effects on intracellular pH. Embo J 1993; 12: 5209–5218
   PubMed Web of Science ®Google Scholar
• Denker SP, Huang DC, Orlowski J, Furthmayr H, Barber DL. Direct binding of the Na+-H+ exchanger NHE1 to ERM proteins regulates the cortical cytoskeleton and cell shape independently of H+ translocation. Mol Cell 2000; 6: 1425–1436
   PubMed Web of Science ®Google Scholar
• Onishi I, Lin PJ, Diering GH, Williams WP, Numata M. RACK1 associates with NHE5 in focal adhesions and positively regulates the transporter activity. Cell Signal 2007; 19: 194–203
   Google Scholar
• Kreis S, Schonfeld HJ, Melchior C, Steiner B, Kieffer N. The intermediate filament protein vimentin binds specifically to a recombinant integrin alpha2/beta1 cytoplasmic tail complex and co-localizes with native alpha2/beta1 in endothelial cell focal adhesions. Exp Cell Res 2005; 305: 110–121
   PubMed Web of Science ®Google Scholar
• Tsuruta D, Jones JC. The vimentin cytoskeleton regulates focal contact size and adhesion of endothelial cells subjected to shear stress. J Cell Sci 2003; 116: 4977–4984
   PubMed Web of Science ®Google Scholar
• Eckes B, Dogic D, Colucci-Guyon E, Wang N, Maniotis A, Ingber D, Merckling A, Langa F, Aumailley M, Delouvee A, Koteliansky V, Babinet C, Krieg T. Impaired mechanical stability, migration and contractile capacity in vimentin-deficient fibroblasts. J Cell Sci 1998; 111: 1897–1907
   PubMed Web of Science ®Google Scholar
• Nieminen M, Henttinen T, Merinen M, Marttila-Ichihara F, Eriksson JE, Jalkanen S. Vimentin function in lymphocyte adhesion and transcellular migration. Nat Cell Biol 2006; 8: 156–162
   PubMed Web of Science ®Google Scholar
• Ivaska J, Vuoriluoto K, Huovinen T, Izawa I, Inagaki M, Parker PJ. PKCepsilon-mediated phosphorylation of vimentin controls integrin recycling and motility. Embo J 2005; 24: 3834–3845
   PubMed Web of Science ®Google Scholar
• Liao HX, Lee DM, Levesque MC, Haynes BF. N-terminal and central regions of the human CD44 extracellular domain participate in cell surface hyaluronan binding. J Immunol 1995; 155: 3938–3945
   PubMed Web of Science ®Google Scholar
• Yang B, Yang BL, Savani RC, Turley EA. Identification of a common hyaluronan binding motif in the hyaluronan binding proteins RHAMM, CD44 and link protein. Embo J 1994; 13: 286–296
   PubMed Web of Science ®Google Scholar
• Orian-Rousseau V, Chen L, Sleeman JP, Herrlich P, Ponta H. CD44 is required for two consecutive steps in HGF/c-Met signaling. Genes Dev 2002; 16: 3074–3086
   PubMed Web of Science ®Google Scholar
• Stapleton G, Malliri A, Ozanne BW. Downregulated AP-1 activity is associated with inhibition of Protein-Kinase-C-dependent CD44 and ezrin localisation and upregulation of PKC theta in A431 cells. J Cell Sci 2002; 115: 2713–2724
   PubMedGoogle Scholar
• Legg JW, Lewis CA, Parsons M, Ng T, Isacke CM. A novel PKC-regulated mechanism controls CD44 ezrin association and directional cell motility. Nat Cell Biol 2002; 4: 399–407
   PubMed Web of Science ®Google Scholar
• Sheng M, Sala C. PDZ domains and the organization of supramolecular complexes. Annu Rev Neurosci 2001; 24: 1–29
   PubMed Web of Science ®Google Scholar
• Bourguignon LY, Singleton PA, Diedrich F, Stern R, Gilad E. CD44 interaction with Na+ − H+ exchanger (NHE1) creates acidic microenvironments leading to hyaluronidase-2 and cathepsin B activation and breast tumor cell invasion. J Biol Chem 2004; 279: 26991–27007
   PubMed Web of Science ®Google Scholar
• Runembert I, Queffeulou G, Federici P, Vrtovsnik F, Colucci-Guyon E, Babinet C, Briand P, Trugnan G, Friedlander G, Terzi F. Vimentin affects localization and activity of sodium-glucose cotransporter SGLT1 in membrane rafts. J Cell Sci 2002; 115: 713–724
   PubMed Web of Science ®Google Scholar
• Sprenger RR, Fontijn RD, Marle J, Pannekoek H, Horrevoets AJG. Spatial segregation of transport and signalling functions between human endothelial caveolae and lipid raft proteomes. Biochem J 2006; 400: 401–410
   PubMed Web of Science ®Google Scholar
• Wang H, Haas M, Liang M, Cai T, Tian J, Li S, Xie Z. Ouabain assembles signaling cascades through the caveolar Na+/K+-ATPase. J Biol Chem 2004; 279: 17250–17259
   PubMed Web of Science ®Google Scholar