Fluorescent neoglycolipids. Improved probes for oligosaccharide ligand discovery
- PMID: 10712612
- DOI: 10.1046/j.1432-1327.2000.01178.x
Fluorescent neoglycolipids. Improved probes for oligosaccharide ligand discovery
Abstract
A second generation of lipid-linked oligosaccharide probes, fluorescent neoglycolipids, has been designed and synthesized for ligand discovery within highly complex mixtures of oligosaccharides. The aminolipid 1,2-dihexadecyl-sn-glycero-3-phosphoethanolamine (DHPE), which has been used extensively to generate neoglycolipids for biological and structural studies, has been modified to incorporate a fluorescent label, anthracene. This new lipid reagent, N-aminoacetyl-N-(9-anthracenylmethyl)-1, 2-dihexadecyl-sn-glycero-3-phosphoethanolamine (ADHP), synthesized from anthracenaldehyde and DHPE gives an intense fluorescence under UV light. Fluorescent neoglycolipids derived from a variety of neutral and acidic oligosaccharides by conjugation to ADHP, by reductive amination, can be detected and quantified by spectrophotometry and scanning densitometry, and resolved by TLC and HPLC with subpicomole detection. Antigenicities of the ADHP-neoglycolipids are well retained, and picomole levels can be detected using monoclonal carbohydrate sequence-specific antibodies. Among O-glycans from an ovarian cystadenoma mucin, isomeric oligosaccharide sequences, sialyl-Lea- and sialyl-Lex-active, could be resolved by HPLC as fluorescent neoglycolipids, and sequenced by liquid secondary-ion mass spectrometry. Thus the neoglycolipid technology now uniquely combines high sensitivity of immuno-detection with a comparable sensitivity of chemical detection. Principles are thus established for a streamlined technology whereby an oligosaccharide population is carried through ligand detection and ligand isolation steps, and sequence determination by mass spectrometry, enzymatic sequencing and other state-of-the-art technologies for carbohydrate analysis.
Similar articles
-
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. 1997 Sep;7(6):861-72. doi: 10.1093/glycob/7.6.861. Glycobiology. 1997. PMID: 9376689
-
Microscale sequencing of O-linked oligosaccharides using mild periodate oxidation of alditols, coupling to phospholipid and TLC-MS analysis of the resulting neoglycolipids.Eur J Biochem. 1990 May 20;189(3):499-507. doi: 10.1111/j.1432-1033.1990.tb15515.x. Eur J Biochem. 1990. PMID: 2161756
-
TLC-LSIMS of neoglycolipids of glycosaminoglycan disaccharides and of oxymercuration cleavage products of heparin fragments that contain unsaturated uronic acid.Carbohydr Res. 1995 Apr 3;269(1):111-24. doi: 10.1016/0008-6215(94)00350-o. Carbohydr Res. 1995. PMID: 7773985
-
'Glyco-epitope' assignments for the selectins: advances enabled by the neoglycolipid (NGL) technology in conjunction with synthetic carbohydrate chemistry.Adv Exp Med Biol. 2001;491:65-78. doi: 10.1007/978-1-4615-1267-7_5. Adv Exp Med Biol. 2001. PMID: 14533790 Review.
-
Carbohydrate recognition in the immune system: contributions of neoglycolipid-based microarrays to carbohydrate ligand discovery.Ann N Y Acad Sci. 2013 Jul;1292(1):33-44. doi: 10.1111/nyas.12210. Epub 2013 Jul 8. Ann N Y Acad Sci. 2013. PMID: 23834439 Free PMC article. Review.
Cited by
-
Carbohydrate sequence of the prostate cancer-associated antigen F77 assigned by a mucin O-glycome designer array.J Biol Chem. 2014 Jun 6;289(23):16462-77. doi: 10.1074/jbc.M114.558932. Epub 2014 Apr 21. J Biol Chem. 2014. PMID: 24753245 Free PMC article.
-
Shotgun glycomics: a microarray strategy for functional glycomics.Nat Methods. 2011 Jan;8(1):85-90. doi: 10.1038/nmeth.1540. Epub 2010 Dec 5. Nat Methods. 2011. PMID: 21131969 Free PMC article.
-
O-Glycome Beam Search Arrays for Carbohydrate Ligand Discovery.Mol Cell Proteomics. 2018 Jan;17(1):121-133. doi: 10.1074/mcp.RA117.000285. Epub 2017 Nov 28. Mol Cell Proteomics. 2018. PMID: 29183914 Free PMC article.
-
A Cytotoxic Antibody Recognizing Lacto-N-fucopentaose I (LNFP I) on Human Induced Pluripotent Stem (hiPS) Cells.J Biol Chem. 2015 Aug 14;290(33):20071-85. doi: 10.1074/jbc.M115.657692. Epub 2015 Jun 22. J Biol Chem. 2015. PMID: 26100630 Free PMC article.
-
Avidity of α-fucose on human milk oligosaccharides and blood group-unrelated oligo/polyfucoses is essential for potent norovirus-binding targets.J Biol Chem. 2018 Jul 27;293(30):11955-11965. doi: 10.1074/jbc.RA117.001369. Epub 2018 Jun 1. J Biol Chem. 2018. PMID: 29858242 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources