Tumor-Associated SLex-Lex Antigen Production Service

Tumor-Associated SLex-Lex Antigen Production Service at CD BioGlyco

SLex-Lex is an important biomolecule that plays an essential role in processes such as cancer metastasis and inflammation. However, the complexity and rarity of its chemical structure make its study challenging. To better address your research questions, CD BioGlyco utilizes our specialized Glyco™ Vaccine Development Platform to offer a full range of Tumor-Associated Glycolipid Antigen Production Services, including tumor-associated sLex-Lex antigen production service. Simply tell us your project goals and we will complete all the following experiments.

  • Chemical synthesis

We synthesize the target molecule, sLex-Lex antigen, through a chemical process that involves connecting two sugar chain structures: sLex and Lex. The process requires the design and optimization of a multi-step reaction pathway involving the synthesis of sLex and Lex monomers, protecting group introduction and removal, and the linking of the two monomers to ultimately yield the target compound sLex-Lex antigen.

  • Enzyme-catalyzed synthesis

We accomplish the synthesis of sLex-Lex antigens under relatively mild conditions by using enzymatic catalysts such as glycosyltransferases, glycosyltransferase mimics, or polysaccharide synthases, and controlling the reaction conditions and catalytic mechanism.

Fig.1 Technologies in tumor-associated SLex-Lex antigen production. (CD BioGlyco) Fig.1 Technologies in tumor-associated SLex-Lex antigen production. (CD BioGlyco)

SLex-Lex antigens are commonly expressed on the surface of tumor cells and play an essential role in tumor invasion and metastasis. Therefore, we provide the follow-up sLex-Lex antigen anti-tumor vaccine development services to advance your cancer-related research.

Applications

  • Levels of sLex-Lex antigen can be detected in blood or urine and can therefore be used for early detection and assessment of tumors.
  • SLex-Lex antigen is considered to be a potent tumor-specific antigen and synthesis or extraction of it from tumor cells can be used to design cancer vaccines.

Publication

Doi: 10.1021/ja00034a063

Journal: Journal of the American Chemical Society

Abstract: This article describes a chemical method for the synthesis of the disaccharide antigen sialyl dimeric Lex (sdiLex), which can be synthesized by total synthesis to obtain sufficient quantities of sdiLex, providing an important tool and material for related research.

Method: The authors utilized phenylthio groups as cofactors to facilitate and stereochemically control the formation of two monomers. Rapid, convergent assembly of the desired backbone was achieved by stereocontrolled construction of three specified glycosidic bonds, followed by deprotection to yield the product.

Fig.2 Structures of natural sialyl di-Lex 1 and derivative 2. (Nicolaou, et al., 2011) Fig.2 Structures of natural sdiLex 1 and derivative 2. (Nicolaou, et al., 2011)

Frequently Asked Question

  • What is the structure of the sLex-Lex antigen?

The sLex-Lex antigen is a disaccharide antigen consisting of two monosaccharide residues, sLex and Lex, through specific linkages. In particular, the sLex structure contains a NeuAcα2-3Galβ1-4(Fucα1-3)GlcNAc unit and a Galβ1-4(Fucα1-3)GlcNAc unit. The Lex structure consists of a Galβ1-4(Fucα1-3)GlcNAc unit. SLex and Lex are linked together through the β1-4 bond of Gal residue, which together form the sLex - Lex antigen.

  • How is the sLex-Lex antigen expressed through cell surface glycan groups?

The synthesis of sLex-Lex antigen is associated with glycosyltransferases that catalyze the addition and attachment of monosaccharide residues to form the specific sugar chain structure of sLex-Lex antigen.

At CD BioGlyco, our experienced scientists take care of all tumor-associated sLex-Lex antigen production services, allowing clients to fully rely on the resultant data without having to invest extra time in antigen production or expensive laboratory equipment. For further details, please don't hesitate to contact us.

Reference

  1. Nicolaou, K.C.; et al. Total synthesis of sialyl dimeric Lex. Journal of the American Chemical Society. 1992, 114(8): 3126-3128.
This service is for Research Use Only, not intended for any clinical use.

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