Various species of Leishmania cause leishmaniasis, which is transmitted through the bites of sandflies. The surface of Leishmania parasites is covered with multiple proteins and glycoproteins, including gp63, lipophosphoglycan (LPG), and promastigote surface antigen (PSA). Leishmania utilizes multiple receptor-mediated entry pathways to enter the host. GP63 is highly expressed in promastigotes and converts C3 opsonin to C3b (the natural ligand of the first complement receptor (CR1)). GP63 also binds fibronectin, bridging the parasite to the fibronectin receptors (FnRs). Mannose receptor (MR) identifies terminal sugar residues on LPG. LPG expression on amastigotes is not as strong as on promastigotes, allowing barely expressed GP63 to access the C3 protein and subsequently the third complement receptor (CR3). Antibody and fibronectin detection of amastigotes results in the ligation of Fc gamma receptors (FcγRs) and FnR, respectively.
Fig.1 Receptors for Leishmania entry into host phagocytes. (Ueno & Wilson, 2012)
LPG is a complex glycolipid molecule Leishmania parasite surface-based, and the Leishmania parasite repeating phosphodisaccharide is a specific phosphodisaccharide unit that appears repeatedly in the LPG molecule. CD BioGlyco provides specialized Leishmania parasite repeating phosphodisaccharide production services to support vaccine research.
CD BioGlyco uses chemical synthesis methods to synthesize the repeated phosphodisaccharides of Leishmania parasites. The phosphodisaccharide units are connected to adjacent sugar units (such as glucose, mannose, and galactose) through glycosidic bonds or phosphodisaccharide bonds to form a chain structure. Phosphate groups confer specific chemical properties and biological activities to these polysaccharide molecules, affecting their function and interactions in biological systems.
CD BioGlyco uses various chromatography techniques (such as gel chromatography, and high-performance liquid chromatography) to separate and purify the synthesized repeating phosphodisaccharides to obtain high-purity target products.
CD BioGlyco uses advanced analytical techniques to conduct structural verification of the synthesized repeating phosphodisaccharides, which helps confirm that the products provided meet the target requirements.
CD BioGlyco provides production for Leishmania parasite repeating phosphodisaccharides of different lengths, modification methods, and structures according to client needs. We flexibly adjust synthesis strategies to meet specific requirements.
CD BioGlyco evaluates the immunogenicity and protective effects of synthetic repeating phosphodisaccharides in animal models or in vitro experiments, which facilitates the screening of vaccine candidates and further advances the development of vaccines. Moreover, we have established the world's leading Glyco™ Vaccine Development Platform, and provide vaccine development services based on Leishmania parasites repeating phosphodisaccharide.
Fig.2 Leishmania parasites repeating phosphodisaccharide production services. (CD BioGlyco)
CD BioGlyco has a professional technical team engaged in the production of Leishmania parasites repeating phosphodisaccharides, which provide efficient and high-quality phosphodisaccharides for vaccine development. Please feel free to contact us quickly if you would like to acquire detailed information.
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