Marine lipopolysaccharide (LPS) has specific biological activities. For example, it is involved in bacterial survival in many hosts, has antigenic properties, as well as being involved in serological specificity, etc. Therefore, the development of vaccines centered on marine LPS with properties that attenuate bacterial virulence or increase the body's immunity is promising for research. At CD BioGlyco, we propose a comprehensive marine LPS vaccine development service in the context of Developing Marine Carbohydrate Vaccines.
First, we dissolve marine LPS in an organic solvent, and after a period of agitation and several dialysis, the solution is centrifuged. Then, the supernatant is freeze-dried to obtain the desired LPS immunogen. In addition, we use a gel chromatography column for further purification.
First, we react to the terminal residues of marine LPS with differently designed bifunctional linkers. Then, they are reacted with residues of carrier proteins to form marine LPS-linker-protein couplers. In this method, we also utilize a site-selective modification approach to ensure that the couplers have the most binding sites.
In addition, we offer analysis of coupling compounds:
We prepare the vaccine by mixing immunogenic marine LPS coupling with stabilizers, emulsifiers, and adjuvants. Next, we provide mice immunization assays to analyze the ability of the vaccine to induce antibodies. We also provide enzyme-linked immunosorbent assay (ELISA) to analyze the effectiveness of the vaccine.
Fig.1 Marine LPS-based vaccine development services. (CD BioGlyco)
Technology: Decarboxylation amidation, SDS-PAGE, ELISA, Immunoassay
Journal: Journal of Biomedical Science
IF: 11.0
Published: 2020
Results: The authors characterized the synthesized coupled vaccine using SDS-PAGE and FPLC. Their polysaccharide and protein contents were also determined. ELISA showed that when mice were immunized with a 2.5 μg dose of lipid-A free lipopolysaccharide (LFPS) conjugate vaccine, serum immunoglobulin G against S. Typhimurium LPS was elicited. In addition, the straight-chain amide linker in the conjugate did not interfere with the desired immune response. Second, vaccines derived from unisolated LFPS or high-quality fractions showed the same effect in inducing serum immunoglobulin G antibodies. Evaluation of the efficacy of the vaccine indicated that when S. Typhimurium flagellin (FliC) was used as the adjuvant protein carrier, the vaccine was 74% effective and the survival rate of the mice was 80% on day 28 after tapping.
Fig.2 Design of polysaccharide–protein vaccine. (Chiu, et al., 2020)
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for more information on the vaccine development of marine carbohydrates.References