α-Gal Lewis X (Galα1-3Glcβ1-3(Fucα1-4)GlcNAc) is a branched trisaccharide combining α-Gal epitope with Lewis X core, naturally occurring in mammalian glycoconjugates and tumor-associated antigens, synthesized as white powder for xenoantigen research, cancer diagnostics, and immunology. This structure (Gal α1-3 linked to Glc β1-3(Fuc α1-4)GlcNAc) elicits strong anti-Gal antibody binding while mimicking selectin ligands, aiding in studies of inflammation, metastasis, and xenotransplantation rejection; commercially available >90% pure via enzymatic synthesis, stable lyophilized at -20°C for multi-year use, with key roles in pathogen adhesion inhibition and glycan array standards.
Appearance
- White to off-white amorphous powder or lyophilized solid.
- Highly water-soluble (>50 g/L); no distinct melting point reported.
Source
- Endogenous in porcine/xenogeneic tissues, human tumors, and select mucins.
- Microbial/enzymatic production using fucosyl-/galactosyl-transferases on Lewis X acceptors.
Molecular Weight and Structure
- Molecular mass 489.47 g/mol, formula C₁₉H₃₄NO₁₅ (core trisaccharide).
- Galα1-3Glcβ1-3(Fucα1-4)GlcNAc with branched α-Gal on reducing GlcNAc arm.
Sugar Specificity
- Recognized by anti-α-Gal IgM/G, DC-SIGN, and selectins via Galα1-3 and Fucα1-4.
- Cleaved by α1-3 galactosidases and α1-4 fucosidases from Bifidobacterium spp.
Biological Activity
- Triggers hyperacute rejection in xenotransplants; promotes tumor metastasis via E-selectin.
- Inhibits bacterial adhesion (e.g., H. pylori); modulates inflammation and α-Gal syndrome.
Purity and Microbial Contamination
90-95% by NMR/HPLC; endotoxins <10 EU/mg.
- Pathogen-free, heavy metals < ICH limits, moisture <5% lyophilized.
Identity and Quality Control
- ¹H-NMR for linkage confirmation; MALDI-TOF MS for mass; HPAEC for purity.
- Monosaccharide analysis by GC-MS; COA per batch.
Shelf Life and Storage
- 2-3 years at -20°C lyophilized under argon.
- Short-term at 4°C; protect from moisture/hydrolases.
Applications
- Xenograft antigen standards, cancer biomarker assays, selectin inhibitors.
- Glycan microarrays, vaccine design, anti-metastatic therapeutics.
Key Characteristics
- Acid-stable to stomach; colonic utilization; dual epitope for precise targeting.
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