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Volumn 13, Issue 5, 2003, Pages 637-645

Carbohydrate microarrays - A new set of technologies at the frontiers of glycomics

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY; CARBOHYDRATE; CARBOHYDRATE BINDING PROTEIN; CHEMOKINE; CYTOKINE; GLYCOCONJUGATE; LIGAND; MONOSACCHARIDE; OLIGOSACCHARIDE; PLANT LECTIN; SELECTIN;

EID: 0141953233     PISSN: 0959440X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.sbi.2003.09.002     Document Type: Review
Times cited : (289)

References (53)
  • 2
    • 0027519943 scopus 로고
    • Protein glycosylation. Structural and functional aspects
    • Lis H., Sharon N. Protein glycosylation. Structural and functional aspects. Eur J Biochem. 218:1993;1-27.
    • (1993) Eur J Biochem , vol.218 , pp. 1-27
    • Lis, H.1    Sharon, N.2
  • 3
    • 0031820273 scopus 로고    scopus 로고
    • The C-type lectin superfamily in the immune system
    • Weis W.I., Taylor M.E., Drickamer K. The C-type lectin superfamily in the immune system. Immunol Rev. 163:1998;19-34.
    • (1998) Immunol Rev , vol.163 , pp. 19-34
    • Weis, W.I.1    Taylor, M.E.2    Drickamer, K.3
  • 5
    • 0035937505 scopus 로고    scopus 로고
    • Intracellular functions of N-linked glycans
    • Helenius A., Aebi M. Intracellular functions of N-linked glycans. Science. 291:2001;2364-2369.
    • (2001) Science , vol.291 , pp. 2364-2369
    • Helenius, A.1    Aebi, M.2
  • 7
    • 0036481121 scopus 로고    scopus 로고
    • C-type lectin receptors on dendritic cells and Langerhans cells
    • Figdor C.G., van Kooyk Y., Adema G.J. C-type lectin receptors on dendritic cells and Langerhans cells. Nat Rev Immunol. 2:2002;77-84.
    • (2002) Nat Rev Immunol , vol.2 , pp. 77-84
    • Figdor, C.G.1    Van Kooyk, Y.2    Adema, G.J.3
  • 8
    • 0034442863 scopus 로고    scopus 로고
    • Progress in deciphering the information content of the 'glycome'-a crescendo in the closing years of the millennium
    • Feizi T. Progress in deciphering the information content of the 'glycome'-a crescendo in the closing years of the millennium. Glycoconj J. 17:2000;553-565.
    • (2000) Glycoconj J , vol.17 , pp. 553-565
    • Feizi, T.1
  • 9
    • 0028806048 scopus 로고
    • Quantitative monitoring of gene expression patterns with a complementary DNA microarray
    • Schena M., Shalon D., Davis R.W., Brown P.O. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science. 270:1995;467-470.
    • (1995) Science , vol.270 , pp. 467-470
    • Schena, M.1    Shalon, D.2    Davis, R.W.3    Brown, P.O.4
  • 10
    • 0036199586 scopus 로고    scopus 로고
    • A perspective on protein microarrays
    • Mitchell P. A perspective on protein microarrays. Nat Biotechnol. 20:2002;225-229.
    • (2002) Nat Biotechnol , vol.20 , pp. 225-229
    • Mitchell, P.1
  • 11
    • 37049091331 scopus 로고
    • Synthesis of blood-group substances. Part 7. Synthesis of the branched trisaccharide O-a-L-fucopyranosyl-(1-3)-[O.B.D.galactopyranosyl-(1-4)] -2-acetamido-w-deoxy-D-glucopyrano se
    • Jacquinet J.-C., Sinay P. Synthesis of blood-group substances. Part 7. Synthesis of the branched trisaccharide O-a-L-fucopyranosyl-(1-3)-[O.B.D.galactopyranosyl-(1-4)] -2-acetamido-w-deoxy-D-glucopyrano se. J Chem Soc Perkin Trans. 1:1979;314-318.
    • (1979) J Chem Soc Perkin Trans , vol.1 , pp. 314-318
    • Jacquinet, J.-C.1    Sinay, P.2
  • 12
    • 0022636075 scopus 로고
    • New methods for the synthesis of glycosides and oligosaccharides-are there alternatives to the Koenigs-Knorr method
    • Schmidt R.R. New methods for the synthesis of glycosides and oligosaccharides-are there alternatives to the Koenigs-Knorr method. Angew Chem Int Ed Engl. 25:1986;212-235.
    • (1986) Angew Chem Int Ed Engl , vol.25 , pp. 212-235
    • Schmidt, R.R.1
  • 13
    • 0025708611 scopus 로고
    • Syntheses of linear tetra-, hexa-, and octa-saccharide fragments of the i-blood group active poly-(N-acetyl-lactosamine) series. Blockwise methods for the synthesis of repetitive oligosaccharide sequences
    • Alais J., Veyrieres A. Syntheses of linear tetra-, hexa-, and octa-saccharide fragments of the i-blood group active poly-(N-acetyl-lactosamine) series. Blockwise methods for the synthesis of repetitive oligosaccharide sequences. Carbohydr Res. 207:1990;11-31.
    • (1990) Carbohydr Res , vol.207 , pp. 11-31
    • Alais, J.1    Veyrieres, A.2
  • 15
    • 33748601612 scopus 로고    scopus 로고
    • Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesis
    • Douglas N.L., Ley S.V., Lucking U., Warriner S.L.L. Tuning glycoside reactivity: new tool for efficient oligosaccharide synthesis. J Chem Soc Perkin Trans. 1:1998;51-65.
    • (1998) J Chem Soc Perkin Trans , vol.1 , pp. 51-65
    • Douglas, N.L.1    Ley, S.V.2    Lucking, U.3    Warriner, S.L.L.4
  • 16
    • 0035805264 scopus 로고    scopus 로고
    • Adventures in carbohydrate chemistry: New synthetic technologies, chemical synthesis, molecular design, and chemical biology
    • Nicolaou K.C., Mitchell H.J. Adventures in carbohydrate chemistry: new synthetic technologies, chemical synthesis, molecular design, and chemical biology. Angew Chem Int Ed Engl. 40:2001;1576-1624.
    • (2001) Angew Chem Int Ed Engl , vol.40 , pp. 1576-1624
    • Nicolaou, K.C.1    Mitchell, H.J.2
  • 17
    • 0032718365 scopus 로고    scopus 로고
    • Synthesis and biological activity of glycolipids, with a focus on gangliosides and sulfatide analogs
    • Ikami T., Ishida H., Kiso M. Synthesis and biological activity of glycolipids, with a focus on gangliosides and sulfatide analogs. Methods Enzymol. 311:2000;547-568.
    • (2000) Methods Enzymol , vol.311 , pp. 547-568
    • Ikami, T.1    Ishida, H.2    Kiso, M.3
  • 18
    • 0035936861 scopus 로고    scopus 로고
    • Automated solid-phase synthesis of oligosaccharides
    • Plante O.J., Palmacci E.R., Seeberger P.H. Automated solid-phase synthesis of oligosaccharides. Science. 291:2001;1523-1527.
    • (2001) Science , vol.291 , pp. 1523-1527
    • Plante, O.J.1    Palmacci, E.R.2    Seeberger, P.H.3
  • 20
    • 0035794984 scopus 로고    scopus 로고
    • Synthesis of the globo H hexasaccharide using the programmable reactivity-based one-pot strategy
    • Burkhart F., Zhang Z., Wacowich-Sgarbi S., Wong C.H. Synthesis of the globo H hexasaccharide using the programmable reactivity-based one-pot strategy. Angew Chem Int Ed Engl. 40:2001;1274-1277.
    • (2001) Angew Chem Int Ed Engl , vol.40 , pp. 1274-1277
    • Burkhart, F.1    Zhang, Z.2    Wacowich-Sgarbi, S.3    Wong, C.H.4
  • 21
    • 85047698715 scopus 로고    scopus 로고
    • Reactivity-based one-pot synthesis of a Lewis Y carbohydrate hapten: A colon-rectal cancer antigen determinant
    • Mong K.K., Wong C.H. Reactivity-based one-pot synthesis of a Lewis Y carbohydrate hapten: a colon-rectal cancer antigen determinant. Angew Chem Int Ed Engl. 41:2002;4087-4090.
    • (2002) Angew Chem Int Ed Engl , vol.41 , pp. 4087-4090
    • Mong, K.K.1    Wong, C.H.2
  • 22
    • 0035843122 scopus 로고    scopus 로고
    • Enzymes for chemical synthesis
    • Koeller K.M., Wong C.H. Enzymes for chemical synthesis. Nature. 409:2001;232-240.
    • (2001) Nature , vol.409 , pp. 232-240
    • Koeller, K.M.1    Wong, C.H.2
  • 23
    • 0032503519 scopus 로고    scopus 로고
    • Glycosynthases: Mutant glycosidases for oligosaccharide synthesis
    • Mackenzie L.F., Wang Q., Warren R.A.J., Withers S.G. Glycosynthases: mutant glycosidases for oligosaccharide synthesis. J Am Chem Soc. 120:1998;5583-5584.
    • (1998) J Am Chem Soc , vol.120 , pp. 5583-5584
    • Mackenzie, L.F.1    Wang, Q.2    Warren, R.A.J.3    Withers, S.G.4
  • 24
    • 0028261414 scopus 로고
    • Enzymatic deglycosylation of asparagine-linked glycans: Purification, properties, and specificity of oligosaccharide-cleaving enzymes from Flavobacterium meningosepticum
    • Tarentino A.L., Plummer T.H. Jr. Enzymatic deglycosylation of asparagine-linked glycans: purification, properties, and specificity of oligosaccharide-cleaving enzymes from Flavobacterium meningosepticum. Methods Enzymol. 230:1994;44-57.
    • (1994) Methods Enzymol , vol.230 , pp. 44-57
    • Tarentino, A.L.1    Plummer T.H., Jr.2
  • 25
    • 0020020233 scopus 로고
    • Hydrazinolysis of asparagine-linked sugar chains to produce free oligosaccharides
    • Takasaki S., Mizuochi T., Kobata A. Hydrazinolysis of asparagine-linked sugar chains to produce free oligosaccharides. Methods Enzymol. 83:1982;263-268.
    • (1982) Methods Enzymol , vol.83 , pp. 263-268
    • Takasaki, S.1    Mizuochi, T.2    Kobata, A.3
  • 26
    • 0030883428 scopus 로고    scopus 로고
    • Nonreductive release of O-linked oligosaccharides from mucin glycoproteins for structure/function assignments as neoglycolipids: Application in the detection of novel ligands for E-selectin
    • Chai W., Feizi T., Yuen C.-T., Lawson A.M. Nonreductive release of O-linked oligosaccharides from mucin glycoproteins for structure/function assignments as neoglycolipids: application in the detection of novel ligands for E-selectin. Glycobiology. 7:1997;861-872.
    • (1997) Glycobiology , vol.7 , pp. 861-872
    • Chai, W.1    Feizi, T.2    Yuen, C.-T.3    Lawson, A.M.4
  • 27
    • 0027441378 scopus 로고
    • Use of hydrazine to release in intact and unreduced form both N- and O-linked oligosaccharides from glycoproteins
    • Patel T., Bruce J., Merry A., Bigge C., Wormald M., Jaques A., Parekh R. Use of hydrazine to release in intact and unreduced form both N- and O-linked oligosaccharides from glycoproteins. Biochemistry. 32:1993;679-693.
    • (1993) Biochemistry , vol.32 , pp. 679-693
    • Patel, T.1    Bruce, J.2    Merry, A.3    Bigge, C.4    Wormald, M.5    Jaques, A.6    Parekh, R.7
  • 29
    • 0032523417 scopus 로고    scopus 로고
    • Characterization of heparin oligosaccharide mixtures as ammonium salts using electrospray mass spectrometry
    • Chai W., Luo J., Lim C.K., Lawson A.M. Characterization of heparin oligosaccharide mixtures as ammonium salts using electrospray mass spectrometry. Anal Chem. 70:1998;2060-2066.
    • (1998) Anal Chem , vol.70 , pp. 2060-2066
    • Chai, W.1    Luo, J.2    Lim, C.K.3    Lawson, A.M.4
  • 30
    • 0017189425 scopus 로고
    • Formation of anhydrosugars in the chemical depolymerization of heparin
    • Shively J.E., Conrad H.E. Formation of anhydrosugars in the chemical depolymerization of heparin. Biochemistry. 15:1976;3932-3942.
    • (1976) Biochemistry , vol.15 , pp. 3932-3942
    • Shively, J.E.1    Conrad, H.E.2
  • 31
    • 0035167226 scopus 로고    scopus 로고
    • Inhibition of adhesion of Plasmodium falciparum-infected erythrocytes by structurally defined hyaluronic acid dodecasaccharides
    • Chai W., Beeson J.G., Kogelberg H., Brown G.V., Lawson A.M. Inhibition of adhesion of Plasmodium falciparum-infected erythrocytes by structurally defined hyaluronic acid dodecasaccharides. Infect Immun. 69:2001;420-425.
    • (2001) Infect Immun , vol.69 , pp. 420-425
    • Chai, W.1    Beeson, J.G.2    Kogelberg, H.3    Brown, G.V.4    Lawson, A.M.5
  • 33
    • 0033152483 scopus 로고    scopus 로고
    • Core-branching pattern and sequence analysis of mannitol-terminating oligosaccharides by neoglycolipid technology
    • Chai W., Yuen C.-T., Feizi T., Lawson A.M. Core-branching pattern and sequence analysis of mannitol-terminating oligosaccharides by neoglycolipid technology. Anal Biochem. 270:1999;314-322.
    • (1999) Anal Biochem , vol.270 , pp. 314-322
    • Chai, W.1    Yuen, C.-T.2    Feizi, T.3    Lawson, A.M.4
  • 34
    • 0014980046 scopus 로고
    • Alkaline borohydride degradation of blood group H substance
    • Iyer R.N., Carlson D.M. Alkaline borohydride degradation of blood group H substance. Arch Biochem Biophys. 142:1971;101-105.
    • (1971) Arch Biochem Biophys , vol.142 , pp. 101-105
    • Iyer, R.N.1    Carlson, D.M.2
  • 35
    • 0031004767 scopus 로고    scopus 로고
    • Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-linked or 2,6-linked hexose (mannose)
    • Yuen C.-T., Chai W., Loveless R.W., Lawson A.M., Margolis R.U., Feizi T. Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-linked or 2,6-linked hexose (mannose). J Biol Chem. 272:1997;8924-8931.
    • (1997) J Biol Chem , vol.272 , pp. 8924-8931
    • Yuen, C.-T.1    Chai, W.2    Loveless, R.W.3    Lawson, A.M.4    Margolis, R.U.5    Feizi, T.6
  • 36
    • 0033179169 scopus 로고    scopus 로고
    • High prevalence of 2-mono- and 2,6-di-substituted mannol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis
    • Chai W., Yuen C.T., Kogelberg H., Carruthers R.A., Margolis R.U., Feizi T., Lawson A.M. High prevalence of 2-mono- and 2,6-di-substituted mannol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis. Eur J Biochem. 263:1999;879-888.
    • (1999) Eur J Biochem , vol.263 , pp. 879-888
    • Chai, W.1    Yuen, C.T.2    Kogelberg, H.3    Carruthers, R.A.4    Margolis, R.U.5    Feizi, T.6    Lawson, A.M.7
  • 37
    • 0036232915 scopus 로고    scopus 로고
    • Carbohydrate arrays for the evaluation of protein binding and enzymatic modification
    • •]).
    • •]).
    • (2002) Chem Biol , vol.9 , pp. 443-454
    • Houseman, B.T.1    Mrksich, M.2
  • 38
    • 0037009016 scopus 로고    scopus 로고
    • Fabrication of carbohydrate chips for studying protein-carbohydrate interactions
    • A microarray is described comprising the monosaccharide N-acetylglucosamine and the disaccharides lactose, cellobiose and maltose, which are covalently attached via maleimide linkers to glass surfaces modified by thiol groups. Three plant lectins are shown to bind to the arrayed carbohydrates in accordance with their known specificities.
    • Park S., Shin I. Fabrication of carbohydrate chips for studying protein-carbohydrate interactions. Angew Chem Int Ed Engl. 41:2002;3180-3182 A microarray is described comprising the monosaccharide N-acetylglucosamine and the disaccharides lactose, cellobiose and maltose, which are covalently attached via maleimide linkers to glass surfaces modified by thiol groups. Three plant lectins are shown to bind to the arrayed carbohydrates in accordance with their known specificities.
    • (2002) Angew Chem Int Ed Engl , vol.41 , pp. 3180-3182
    • Park, S.1    Shin, I.2
  • 39
    • 0036193564 scopus 로고    scopus 로고
    • Carbohydrate microarrays for the recognition of cross-reactive molecular markers of microbes and host cells
    • This is the first published report of a carbohydrate microarray. The arrayed materials are 48 glycoproteins and polysaccharides, each immobilized by noncovalent absorption on nitrocellulose membranes. The microarrays are shown to be well suited to antigenic analyses with monoclonal antibodies and to the detection of antibodies to bacterial polysaccharides in human sera.
    • Wang D., Liu S., Trummer B.J., Deng C., Wang A. Carbohydrate microarrays for the recognition of cross-reactive molecular markers of microbes and host cells. Nat Biotechnol. 20:2002;275-281 This is the first published report of a carbohydrate microarray. The arrayed materials are 48 glycoproteins and polysaccharides, each immobilized by noncovalent absorption on nitrocellulose membranes. The microarrays are shown to be well suited to antigenic analyses with monoclonal antibodies and to the detection of antibodies to bacterial polysaccharides in human sera.
    • (2002) Nat Biotechnol , vol.20 , pp. 275-281
    • Wang, D.1    Liu, S.2    Trummer, B.J.3    Deng, C.4    Wang, A.5
  • 40
    • 0036916176 scopus 로고    scopus 로고
    • Sugar-coated microarrays: A novel slide surface for the high-throughput analysis of glycans
    • The authors describe microarrays of proteoglycans, neoglycoproteins and polysaccharides known to have various degrees and patterns of methyl-esterification, derived from plant cell walls. Hydrophobic polystyrene slides with rough surfaces were used for noncovalent attachment of the carbohydrates. When probed with previously characterized monoclonal antibodies and a phage-derived antibody, the patterns of binding were found to be in accord with their known specificities.
    • Willats W.G., Rasmussen S.E., Kristensen T., Mikkelsen J.D., Knox J.P. Sugar-coated microarrays: a novel slide surface for the high-throughput analysis of glycans. Proteomics. 2:2002;1666-1671 The authors describe microarrays of proteoglycans, neoglycoproteins and polysaccharides known to have various degrees and patterns of methyl-esterification, derived from plant cell walls. Hydrophobic polystyrene slides with rough surfaces were used for noncovalent attachment of the carbohydrates. When probed with previously characterized monoclonal antibodies and a phage-derived antibody, the patterns of binding were found to be in accord with their known specificities.
    • (2002) Proteomics , vol.2 , pp. 1666-1671
    • Willats, W.G.1    Rasmussen, S.E.2    Kristensen, T.3    Mikkelsen, J.D.4    Knox, J.P.5
  • 42
    • 0035990941 scopus 로고    scopus 로고
    • Saccharide display on microtiter plates
    • Conditions are established for fabricating, by noncovalent attachment in plastic microwells, arrays of synthetic carbohydrates linked to an aliphatic hydrocarbon. Galactose and seven di- to hexa-saccharides were derivatized to a 14-carbon aliphatic hydrocarbon and are reported to elicit binding signals in accord with predictions for the three plant lectins investigated.
    • Bryan M.C., Plettenburg O., Sears P., Rabuka D., Wacowich-Sgarbi S., Wong C.H. Saccharide display on microtiter plates. Chem Biol. 9:2002;713-720 Conditions are established for fabricating, by noncovalent attachment in plastic microwells, arrays of synthetic carbohydrates linked to an aliphatic hydrocarbon. Galactose and seven di- to hexa-saccharides were derivatized to a 14-carbon aliphatic hydrocarbon and are reported to elicit binding signals in accord with predictions for the three plant lectins investigated.
    • (2002) Chem Biol , vol.9 , pp. 713-720
    • Bryan, M.C.1    Plettenburg, O.2    Sears, P.3    Rabuka, D.4    Wacowich-Sgarbi, S.5    Wong, C.H.6
  • 44
    • 0032817981 scopus 로고    scopus 로고
    • Influence of oligosaccharide presentation on the interactions of carbohydrate sequence-specific antibodies and the selectins. Observations with biotinylated oligosaccharides
    • Leteux C., Stoll M.S., Childs R.A., Chai W., Vorozhaikina M., Feizi T. Influence of oligosaccharide presentation on the interactions of carbohydrate sequence-specific antibodies and the selectins. Observations with biotinylated oligosaccharides. J Immunol Methods. 227:1999;109-119.
    • (1999) J Immunol Methods , vol.227 , pp. 109-119
    • Leteux, C.1    Stoll, M.S.2    Childs, R.A.3    Chai, W.4    Vorozhaikina, M.5    Feizi, T.6
  • 46
    • 0028201330 scopus 로고
    • Neoglycolipids: Probes of oligosaccharide structure, antigenicity and function
    • Feizi T., Stoll M.S., Yuen C.-T., Chai W., Lawson A.M. Neoglycolipids: probes of oligosaccharide structure, antigenicity and function. Methods Enzymol. 230:1994;484-519.
    • (1994) Methods Enzymol , vol.230 , pp. 484-519
    • Feizi, T.1    Stoll, M.S.2    Yuen, C.-T.3    Chai, W.4    Lawson, A.M.5
  • 48
    • 0029952519 scopus 로고    scopus 로고
    • Structural basis of lectin-carbohydrate recognition
    • Weis W.I., Drickamer K. Structural basis of lectin-carbohydrate recognition. Annu Rev Biochem. 65:1996;441-473.
    • (1996) Annu Rev Biochem , vol.65 , pp. 441-473
    • Weis, W.I.1    Drickamer, K.2
  • 49
    • 0141987855 scopus 로고    scopus 로고
    • New structural insights into carbohydrate-protein interactions from NMR spectroscopy
    • in press
    • Kogelberg H, Solis D, Jimenez-Barbero J: New structural insights into carbohydrate-protein interactions from NMR spectroscopy. Curr Opin Struct Biol 2003, in press.
    • (2003) Curr Opin Struct Biol
    • Kogelberg, H.1    Solis, D.2    Jimenez-Barbero, J.3
  • 50
    • 0035093097 scopus 로고    scopus 로고
    • Carrier protein-modulated presentation and recognition of an N-glycan: Observations on the interactions of Man(8) glycoform of ribonuclease B with conglutinin
    • Solis D., Bruix M., Gonzalez L., Diaz-Maurino T., Rico M., Jimenez-Barbero J., Feizi T. Carrier protein-modulated presentation and recognition of an N-glycan: observations on the interactions of Man(8) glycoform of ribonuclease B with conglutinin. Glycobiology. 11:2001;31-36.
    • (2001) Glycobiology , vol.11 , pp. 31-36
    • Solis, D.1    Bruix, M.2    Gonzalez, L.3    Diaz-Maurino, T.4    Rico, M.5    Jimenez-Barbero, J.6    Feizi, T.7
  • 51
    • 0033549740 scopus 로고    scopus 로고
    • Carbohydrate mimetics: A new strategy for tackling the problem of carbohydrate-mediated biological recognition
    • Sears P., Wong C.H. Carbohydrate mimetics: a new strategy for tackling the problem of carbohydrate-mediated biological recognition. Angew Chem Int Ed Engl. 38:1999;2300-2324.
    • (1999) Angew Chem Int Ed Engl , vol.38 , pp. 2300-2324
    • Sears, P.1    Wong, C.H.2
  • 52
    • 0035937499 scopus 로고    scopus 로고
    • Chemical glycobiology
    • Bertozzi C.R., Kiessling L.L. Chemical glycobiology. Science. 291:2001;2357-2364.
    • (2001) Science , vol.291 , pp. 2357-2364
    • Bertozzi, C.R.1    Kiessling, L.L.2
  • 53
    • 0141995591 scopus 로고    scopus 로고
    • A new kind of carbohydrate array, its use for profiling anti-glycan antibodies, and the discovery of a novel human cellulose-binding antibody
    • in press
    • Schwarz M, Spector L, Gargir A, Shtevi A, Gortler M, Alstock RT, Dukler AA, Dotan N: A new kind of carbohydrate array, its use for profiling anti-glycan antibodies, and the discovery of a novel human cellulose-binding antibody. Glycobiology 2003, in press.
    • (2003) Glycobiology
    • Schwarz, M.1    Spector, L.2    Gargir, A.3    Shtevi, A.4    Gortler, M.5    Alstock, R.T.6    Dukler, A.A.7    Dotan, N.8


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