Synthesis of Robust Oligosaccharides for Applications in Biotechnology and Biomedical Research
Tech ID: 2023-0001
Abstract
Researchers from California State University, Sacramento have developed a method of that makes it very easy to link together two sugars that are either the same or different using a minimum of steps, no protecting group chemistry, efficient and green reaction conditions, and results in good to excellent product yields.
Full Description
We have developed a unique method to synthesize carbohydrate-based glycomimetic compounds using efficient green chemistry methodologies. This includes: no protecting group chemistry, use of water as a solvent in most reactions, use of a single common commercially available starting material to create multiple building blocks for glycomimetic assembly, use of microwave-mediated reactions to speed up reactions, and the use of water-based purification strategies. The molecules derived from the building blocks can be used to synthesize oligomers of a desired chain length for a variety of biotechnology/biomedical applications. The resultant oligomers are also expected to be stable under a variety of different pH environments, as well as in the presence of common degradative enzymes such as amidases and glycosidases. This chemistry can be used on any sugar that has a minimum of one oxidizable carbon to create stable homo- or hetero-oligosaccharides of one’s choosing for a variety of applications. Our method can also be utilized in other applications for the synthesis of robust polymers for use in biotechnology/biomedical applications.
This invention solves a major issue in carbohydrate chemistry, where multiple additional protection/deprotection steps must be employed to provide regioselectivity to the resultant products if a specific glycosidic linkage orientation (alpha- or beta-) is desired. This leads to longer synthetic pathways and lower overall yields. Additionally, unlike other fields of macromolecules like peptides/proteins, or oligo-/polynucleotides, carbohydrate chemistry has not mastered the ability to automate the synthesis of important oligo-/polysaccharides. As we now know, carbohydrates are incredibly important in understanding a variety of biological attributes, including, but not limited to healthy vs. diseased states, or self vs. non-self. This invention can help us move closer to these achievements and move our understanding of biologically relevant oligo-/polysaccharides forward.
Applications
Features/Benefits
Patent Status
Country
Type
Number
Dated
United States of America
Provisional
63464454
05/05/2023
Inventors
Keywords
Biomimetics
Glycomimetics
N-Acetyl Neuraminic Acid
N-Acetyl Neuraminic Acid Oligosaccharides
N-Acylhydrazide
N,N’-Diacylhydrazide
Non-native glycosidic linkages
Sialic Acid
Sialic Acid Glycomimetics
Sialic Acid Oligosaccharides
Sialooligomers
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