GlycoProfile™ Literature

Track and Probe Glycomic Expression

GlycoProfile™ Metabolic Labeling Reagents enable incorporation, expression and detection of unnatural glycoproteins in cells.

Listed below are many references linked to PubMed, where you can find complete abstract information and relevant journal information.

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Title Author / Journal
A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation. Hang, H.C., et al.
Proc Natl Acad Sci U S A. 2003 Dec 9; 100(25): 14846-51.
Incorporation of azides into recombinant proteins for chemoselective modification by the Staudinger ligation. Kiick, K.L., et al.
Proc Natl Acad Sci U S A. 2002 Jan 8; 99(1): 19-24.
Metabolic labeling of glycoproteins with chemical tags through unnatural sialic acid biosynthesis Jacobs, C.L., et al.
Methods Enzymol. 2000; 327: 260-75.
Cell Surface Engineering by a Modified Staudinger Reaction. Saxon, E., et al.
Science. 2000 March 17; 2007-2010.
Investigating Cellular Metabolism of Synthetic Azidosugars with the Staudinger Ligation Saxon, E., et al.
J Am Chem Soc, 2002 Dec 18; 124(50): 14893-902.
Ketone Isosteres of 2-N-Acetamidosugars as Substrates for Metabolic Cell Surface Engineering. Hang, H.C., et al.
J Am Chem Soc. 2001 Feb 14; 123(6): 1242-3.
A Fluorogenic Dye Activated by the Staudinger Ligation. Lemieux G.A., et al.
J Am Chem Soc. 2003 Apr 23; 125(16): 4708-9.
Probing Glycosyltransferase Activities with the Staudinger Ligation . Hang, H.C., et al.
J Am Chem Soc. 2004; 126(1); 6-7
Imaging Cell Surface Glycans with Bioorthogonal Chemical Reporters . Chang, P.V., et al.
J Am Chem Soc. 2007 Jul 11; 129(27): 8400-1.
Constructing Azide-Labeled Cell Surfaces Using Polysaccharide Biosynthetic Pathways. Luchansky, S.J., et al.
Methods in Enzymology. 2003, 362, 249-272.
Metabolic Functionalization of Recombinant Glycoproteins. Luchansky, S.J., et al.
Biochemistry. 2004 Sep 28; 43(38): 12358-66.
Metabolic oligosaccharide engineering as a tool for glycobiology. Danielle, H., et al.
Chem. Bio. 2003, 7, 616-625.
Chemical and biological strategies for engineering cell surface glycosylation. Saxon, E., et al.
Annu. Rev. Cell Dev. Biol. 2001, 17, 1-23
Metabolic substrate engineering as a tool for glycobiology Goon S., Bertozzi, C.R.
J. Carbohydr. Chem. 2002, 21, 943-977
Biochemical engineering of the N-acyl side chain of sialic acid: biological implications. Keppler, O.T., et al.
Glycobiology. 2001 Feb; 11(2): 11R-18R.
A chemical approach for identifying O-GlcNac modified proteins in cells. Vocadlo, D.J., et al.
Proc Natl Acad Sci USA. 1999. Aug 15; 342(Pt 1): 153-61.
Chemical approached to glycobiology: engineering cell surface sialic acids for tumor targeting. Mahal, L.K., et al.
Japan: Gakushin Publishing Company. 1999, 273-280.
Biochemical engineering of surface alpha 2-8 polysialic acid for immunotargeting tumor cells. Keppler, O.T., et al.
Glycobiology. 2001 Feb; 11(2): 11R-18R.
Modulating cell surface immunoreactivity by metabolic induction of unnatural carbohydrate antigens. Goon, .S, et al.
Chem. Biol. 342(Pt 1): 153-61.
Metabolic selection of glycosylation defects in human cells. Yarema, K.J., , et al.
Nat. Biotechnol. 2001 Jun; 19(6): 553-8.
Mechanistic Investigation of the Staudinger Ligation. Lin, F. L., et al.
J. Am. Chem. Soc. 2001 Jun; 19(6): 553-8

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