41744-59-6 , Gala1-3Galb1-4Glc ,
a-Gal epitope type I;
Isoglobotriaose; Linear B-6 trisaccharide;
O-a-D-Galactopyranosyl-(1→3)-O-b-D-galactopyranosyl-(1→4)-D-glucose;
Globoisotriaose
C18H32O16 / 504.44
O-a-D-Galactopyranosyl-(1→3)-O-b-D-galactopyranosyl-(1→4)-D-glucose; Globoisotriaose
Galalpha1-3Galbeta1-4Glc, also known as Gal epitope or alpha-Gal, is a carbohydrate molecule that exists on many mammalian cell surfaces, including those of humans, non-human primates, and Old World monkeys. It was first identified in the 1980s as a major cause of hypersensitivity reactions to animal-derived products, such as red meat and certain medications, in humans. The presence of alpha-Gal on non-primate cells is due to the horizontal transfer of a gene from bacteria, which has evolved as a mechanism for pathogen recognition and immune defense.
Physical and Chemical Properties
Alpha-Gal is a heterodisaccharide composed of two monosaccharides, galactose (Gal) and glucose (Glc), linked by a type II alpha(1,3)-beta(1,4) glycosidic bond. It has a molecular weight of 500-700 g/mol and a bulky structure due to the terminal Gal residue, which protrudes outwards from the cell surface. Alpha-Gal is soluble in water and is stable under physiological conditions.
Synthesis and Characterization
Alpha-Gal can be synthesized enzymatically or chemically using various protocols. The most common method involves the use of alpha1,3-galactosyltransferase (α1,3GT), an enzyme that catalyzes the transfer of Gal from UDP-Gal to a Glc residue on a glycan acceptor. The structure of alpha-Gal can be characterized using various techniques, such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and high-performance liquid chromatography (HPLC).
Analytical Methods
Various analytical methods have been developed to detect and quantify alpha-Gal in different samples, including serum, tissues, and food products. These include enzyme-linked immunosorbent assays (ELISA), Western blotting, flow cytometry, and glycan microarray analysis.
Biological Properties
Alpha-Gal is a potent immunogen that can trigger the production of anti-alpha-Gal antibodies (IgG, IgM, and IgE) in humans and other mammals. These antibodies can recognize and bind to alpha-Gal on cell surfaces, leading to complement activation, cell lysis, and inflammation. The anti-alpha-Gal immune response has been implicated in various physiological and pathological processes, such as transplant rejection, autoimmune diseases, and cancer.
Toxicity and Safety in Scientific Experiments
Alpha-Gal has been extensively studied for its toxicity and safety in scientific experiments, particularly in the fields of xenotransplantation and vaccine development. The presence of alpha-Gal in animal tissues and organs used for transplantation poses a significant risk of hyperacute rejection in humans due to preformed anti-alpha-Gal antibodies. Therefore, strategies to reduce or eliminate alpha-Gal expression in donor animals, such as gene editing and immunosuppressive drugs, have been proposed and tested. In vaccine development, alpha-Gal conjugates have been used as adjuvants to enhance the immunogenicity of antigens. However, their safety and efficacy in humans are still under investigation.
Applications in Scientific Experiments
Alpha-Gal has several applications in scientific experiments, such as cell-based assays, glycan engineering, and glycomics. Its unique structure and immunogenicity make it a useful tool for studying glycan recognition and immune responses. Alpha-Gal can also be engineered into glycan structures to modulate their biological properties or to create novel biomaterials with tunable properties.
Current State of Research
Research on alpha-Gal is ongoing in various fields, including immunology, glycobiology, xenotransplantation, and vaccine development. Some of the current research topics include:
1. Understanding the roles of anti-alpha-Gal antibodies in human diseases, such as cancer and autoimmune disorders.
2. Developing safe and effective methods for alpha-Gal depletion in xenotransplantation.
3. Expanding the applications of alpha-Gal conjugates in vaccine development and cancer immunotherapy.
4. Studying the biosynthesis and regulation of alpha-Gal in different organisms.
Potential Implications in Various Fields of Research and Industry
Alpha-Gal has potential implications in various fields of research and industry, such as:
1. Xenotransplantation: The depletion or modification of alpha-Gal expression in donor animals can enable successful xenotransplantation, which could address the shortage of human organs for transplantation.
2. Vaccine development: Alpha-Gal conjugates can enhance the immune response to antigens and improve the efficacy of vaccines against infectious diseases and cancer.
3. Food industry: The detection and quantification of alpha-Gal in food products can provide valuable information for individuals with alpha-Gal syndrome or other alpha-Gal allergies.
4. Biomaterials: Alpha-Gal can be engineered into glycan structures to create biomaterials with specific properties, such as improved biocompatibility and bioactivity.
Limitations and Future Directions
Despite the significant progress made in alpha-Gal research, several limitations and future directions remain:
1. The mechanisms underlying the immunogenicity and antigenicity of alpha-Gal are not fully understood, and more studies are needed to elucidate these processes.
2. The safety and efficacy of alpha-Gal conjugates and other alpha-Gal-based therapeutics in humans need to be thoroughly evaluated in clinical trials.
3. The potential ecological and public health implications of alpha-Gal depletion in donor animals require careful consideration.
4. The development of novel methods for alpha-Gal synthesis and modification could expand the applications of alpha-Gal in various fields.
CAS Number | 41744-59-6 |
Product Name | Galalpha1-3Galbeta1-4Glc |
IUPAC Name | (2R,3R,4R,5R)-4-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,3,5,6-tetrahydroxyhexanal |
Molecular Formula | C18H32O16 |
Molecular Weight | 504.4 g/mol |
InChI | InChI=1S/C18H32O16/c19-1-5(23)9(25)15(6(24)2-20)33-18-14(30)16(11(27)8(4-22)32-18)34-17-13(29)12(28)10(26)7(3-21)31-17/h1,5-18,20-30H,2-4H2/t5-,6+,7+,8+,9+,10-,11-,12-,13+,14+,15+,16-,17+,18-/m0/s1 |
InChI Key | KZZUYHVLNLDKLB-KXWZGOPVSA-N |
SMILES | C(C1C(C(C(C(O1)OC2C(C(OC(C2O)OC(C(CO)O)C(C(C=O)O)O)CO)O)O)O)O)O |
Canonical SMILES | C(C1C(C(C(C(O1)OC2C(C(OC(C2O)OC(C(CO)O)C(C(C=O)O)O)CO)O)O)O)O)O |
Isomeric SMILES | C([C@@H]1[C@@H]([C@@H]([C@H]([C@H](O1)O[C@H]2[C@H]([C@H](O[C@H]([C@@H]2O)O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)CO)O)O)O)O)O |
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