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2010 | 57 | 1 |

Tytuł artykułu

Analysis of recombinant Duffy protein-linked N-glycans using lectins and glycosidases

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
 Duffy antigen is a glycosylated blood group protein acting as a malarial and chemokine receptor. Using glycosylation mutants we have previously demonstrated, that all three potential glycosylation sites of the Duffy antigen are occupied by N-linked oligosaccharide chains. In this study, wild-type Duffy glycoprotein and three mutants, each containing a single N-glycan, were used to characterize the oligosaccharide chains by lectin blotting and endoglycosidase digestion. The positive reaction of all the recombinant Duffy forms with Datura stramonium and Sambucus nigra lectins showed that each Duffy N-linked glycan contains Galβ1-4GlcNAc units terminated by (α2-6)-linked sialic acid residues, typical of complex oligosaccharides. The reactivity with Aleuria aurantia and Lens culinaris lectins suggested the presence of (α1-6)-linked fucose at the N-glycan chitobiose core. The failure of the Galanthus nivalis and Canavalia ensiformis lectins to bind to any of the Duffy mutants or to the wild-type antigen indicated that none of the three Duffy N-glycosylation sites carries detectable levels of high-mannose oligosaccharide chains. Digestion of Duffy samples with peptide N-glycosidase F and endoglycosidase H confirmed the presence of N-linked complex oligosaccharides. Our results indicate that Duffy antigen N-glycans are mostly core-fucosylated complex type oligosaccharides rich in N-acetyllactosamine and terminated by (α2-6)-linked sialic acid residues.

Wydawca

-

Rocznik

Tom

57

Numer

1

Opis fizyczny

p.49-53,fig.,ref.

Twórcy

autor
  • Polish Academy of Sciences, Wroclaw, Poland
autor
autor

Bibliografia

  • Bannert N, Craig S, Farzan M, Sogah D, Santo NV, Choe H, Sodroski J (2001) Sialylated O-glycans and sulfated tyrosines in the NH2-terminal domain of CC chemokine receptor 5 contribute to high affinity binding of chemokines. J Exp Med 194: 1661-1673.  
  • Bhattacharyya L, Brewer CF (1989) Interactions of concanavalin A with asparagine-linked glycopeptides. Structure/activity relationships of the binding and precipitation of oligomannose and bisected hybrid-type glycopeptides with concanavalin A. Eur J Biochem 178: 721-726.  
  • Blackburn PE, Simpson SV, Nibbs RJB, O'Hara M, Booth R, Poulos J, Isaacs NW, Graham GJ (2004) Purification and biochemical characterization of the D6 chemokine receptor. Biochem J 379: 263-272. 
  • Ciołczyk-Wierzbicka D, Gil D, Hoja-Łukowicz D, Lityńska A, Laidler P (2002) Carbohydrate moieties of N-cadherin from human melanoma cell lines. Acta Biochim Pol 49: 991-998. 
  • Choe H, Moore MJ, Owens C, Wright PL, Vasilieva N, Li W, Singh AP, Shakri R, Chitnis EC, Farzan M (2005) Sulphated tyrosines mediate association of chemokines and Plasmodium vivax Duffy binding protein with the Duffy antigen/receptor for chemokines (DARC). Mol Microbiol 55: 1413-1422. 
  • Czerwiński M, Kern J, Grodecka M, Paprocka M, Krop-Wątorek A, Waśniowska K (2007) Mutational analysis of the N-glycosylation sites of Duffy antigen/receptor for chemokines. Biochem Biophys Res Commun 356: 816-821. 
  • Darbonne WC, Rice GC, Mohler MA, Apple T, Hebert CA, Valente AJ, Baker JB (1991) Red blood cells are a sink for interleukin 8, a leukocyte chemotaxin. J Clin Invest 88: 1362-1367. 
  • Gardner L, Patterson A, Ashot B, Stone M, Middleton J (2004) The human Duffy antigen binds selected inflammatory but not homeostatic chemokines. Biochem Biophys Res Commun 321: 306-312. 
  • Grodecka M, Waśniowska K (2007) Interceptors - "silent" chemokine receptors. Postepy Hig Med Dosw (online) 61: 231-239.
  • Grodecka M, Czerwiński M, Waśniowska K (2008) Analysis of the Duffy glycoprotein N-glycans: use of lectins and glycosidases. Acta Biochim Pol 55 (Suppl 3): P5.1.
  • Gutierrez J, Kremer L, Zaballos A, Goya I, Martinez-A C, Marquez G (2004) Analysis of post-translational CCR8 modifications and their influence on receptor activity. J Biol Chem 279: 14726-14733. 
  • Hadley TJ, Peiper SC (1997) From malaria to chemokine receptor: the emerging physiologic role of the Duffy blood group antigen. Blood 89: 3077-3091.  
  • Hadley TJ, David PH, McGinniss MH, Miller LH (1984) Identification of an erythrocyte component carrying the Duffy blood group Fya antigen. Science 223: 597-599. 
  • He W, Neil S, Kulkarni H, Wright E, Agan BK, Marconi VC, Dolan MJ, Weiss RA, Ahuja SK (2008) Duffy antigen receptor for chemokines mediates trans-infection of HIV-1 from red blood cells to target cells and affects HIV-AIDS susceptibility. Cell Host Microbe 4: 52-62. 
  • Horuk R, Chitnis CE, Darbonne WC, Colby TJ, Rybicki A, Hadley TJ, Miller LH (1993) A receptor for the malarial parasite Plasmodium vivax: The erythrocyte chemokine receptor. Science 261: 1182-1184. 
  • Huskens D, Princen K, Schreiber M, Schols D (2007) The role of N-glycosylation sites on the CXCR4 receptor for CXCL-12 binding and signaling and X4 HIV-1 viral infectivity. Virology 363: 280-287. 
  • Janik ME, Przybyło M, Pocheć E, Pokrywka M, Lityńska A (2010) Effect of α3β1 and αvβ3 integrin glycosylation on interaction of melanoma cells with vitronectin. Acta Biochim Pol 57: 55-61. 
  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of bacteriophage T4. Nature 227: 680-685. 
  • Nibbs R, Graham G, Rot A (2003) Chemokines on the move: control by the chemokine "interceptors" Duffy blood group antigen and D6. Semin Immunol 15: 287-294. 
  • Peiper SC, Wang ZX, Neote K, Martin AW, Showell HJ, Conklyn MJ, Ogborne K, Hadley TJ, Lu ZH, Hesselgesser J, Horuk R (1995) The Duffy antigen/receptor for chemokines (DARC) is expressed in endothelial cells of Duffy negative individuals who lack the erythrocyte receptor. J Exp Med 181: 1311-1317. 
  • Pogo AO, Chaudhuri A (2000) The Duffy protein: A malarial and chemokine receptor. Semin Hematol 37: 122-129. 
  • Preobrazhensky AA, Dragan S, Kawano T, Gavrilin MA, Gulina IV, Chakravarty L, Kolattukudy PE (2000) Monocyte chemotactic protein-1 receptor CCR2B is a glycoprotein that has tyrosine sulfation in a conserved extracellular N-terminal region. J Immunol 165: 5295-5303. 
  • Pruenster M, Mudde L, Bombosi P, Dimitrova S, Zsak M, Middleton J, Richmond A, Graham GJ, Segerer S, Nibbs RJ, Rot A (2008) The Duffy antigen receptor for chemokines transports chemokines and supports their promigratory activity. Nat Immunol 10: 101-108. 
  • Rot A, Horuk R (2009) DARC, the Duffy antigen receptor for chemokines. Methods Enzymol 461: 191-206.  
  • Shen H, Schuster R, Stringer KF, Waltz SE, Lentsch AB (2006) The Duffy antigen/receptor for chemokines (DARC) regulates prostate growth. FASEB J 20: 59-64. 
  • Tanner MJA, Anstee DJ, Mallinson G, Ridgwell K, Martin PG, Avent ND, Parsons SF (1988) Effect of endoglycosidase F-peptidyl N-glycosidase F preparations on the surface components of the human erythrocyte. Carbohydr Res 178: 203-212. 
  • Tournamille C, Colin Y, Cartron JP, Le Van Kim C (1995) Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nat Genet 10: 224-228. 
  • Tournamille C, Le Van Kim C, Gane P, Blanchard D, Proudfoot AE, Cartron JP, Colin Y (1997) Close association of the first and fourth extracellular domains of the Duffy antigen/receptor for chemokines by a disulfide bond is required for ligand binding. J Biol Chem 272: 16274-16280.  
  • Tournamille C, Filipe A, Waśniowska K, Gane P, Lisowska E, Cartron JP, Colin Y, Le Van Kim C (2003) Structure-function analysis of the extracellular domains of the Duffy antigen/receptor for chemokines: characterization of antibody and chemokine binding sites. Br J Haematol 122: 1014-1023. 
  • Towbin H, Staehelin T, Gordon J (1979) Electrophoretic transfer of proteins from polyacrylamide gel to nitrocellulose sheets: Procedure and some applications. Proc Natl Acad Sci USA 76: 4350-4354. 
  • Wang J, Ou ZL, Hou YF, Luo JM, Shen ZZ, Ding J, Shao ZM (2006) Enhanced expression of Duffy antigen receptor for chemokines by breast cancer cells attenuates growth and metastasis potential. Oncogene 25: 7201-7211. 
  • Waśniowska K, Eichenberger P, Kugele F, Hadley TJ (1993) Purification of a 28 kDa non-aggregating tryptic peptide of the Duffy blood group protein. Biochem Biophys Res Commun 192: 366-372.  
  • Waśniowska K, Blanchard D, Janvier D, Wang ZX, Peiper SC, Hadley TH, Lisowska E (1996) Identification of the Fy6 epitope recognized by two monoclonal antibodies in the N-terminal extracellular portion of the Duffy antigen receptor for chemokines. Mol Immunol 33: 917-923. 
  • Waśniowska K, Petit-LeRoux Y, Tournamille C, Le Van Kim C, Cartron JP, Colin Y, Lisowska E, Blanchard D (2002) Structural characterization of the epitope recognized by the new anti-Fy6 monoclonal antibody NaM185-2C3. Transfus Med 12: 205-211. 
  • Winkler CA, An P, Johnson R, Nelson GW, Kirk G (2009) Expression of Duffy antigen receptor for chemokines (DARC) has no effect on HIV-1 acquisition or progression to AIDS in African Americans. Cell Host Microbe 5: 411-413. 
  • Wu AM, Song SC, Tsai MS, Herp A (2001) A guide to the carbohydrate specificities of applied lectins-2 (updated in 2000). Adv Exp Med Biol 491: 551-585. 
  • Wu AM, Lisowska E, Duk M, Yang Z (2008) Lectins as tools in glycoconjugate research. Glycoconj J, doi: 10.1007/s10719-008-9119-7.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-554e8680-2336-4f57-93bd-dd0cf02c2973
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