A research program devoted to the development of new methods for the synthesis of biologically important complex oligosaccharides and glycoconjugates is proposed. Several new methods for glycosidic bond formation will be developed in this granting period. The first is the establishment of the concept of sulfoxide covalent catalysis in the context of dehydrative glycosylation employing 1-hydroxy glycosyl donors. The second reaction is an oxidative glycosylation reaction employing glycal donors. Through the use of hypervalent l(lll) reagents, we intend to establish C2-acyloxyglycosylation as an efficient glycal assembly process for complex carbohydrate synthesis. Investigations into the scope, mechanism, and stereochemical determinants in these new reactions should lead to a series of powerful glycosylation methods that can be applied to the synthesis of natural and non-natural oligosaccharides that are of importance to biology and human medicine. With the use of our glycosylation methodologies, we are in a unique position to perform the first systematic structure-function studies of QS-21 A, a potent immunostimulatory adjuvant used in more than 80 recent and ongoing vaccine clinical trials. Following our recent chemical synthesis of QS-21A, the design and synthesis of several structurally modified/truncated analogs of QS-21A is proposed to generate more potent adjuvants and to probe its unkown mechanism of immunostimulatory activity through SAR studies. We also propose to develop a new strategy for the site selective covalent conjugation of complex carbohydrates with peptides. The efficient synthesis of this class of glycoconjugates will allow for the preparation of diverse glycosylated mucin fragments not only for fundamental studies on mucin glycopeptide architecture, but also for the design of more hydrolytically stable mucin-associated subunit antigens for vaccine therapy. The full development of this research program will expand the repertoire of available carbohydrate synthesis methods and facilitate access to complex carbohydrate immunostimulants for immunological evaluation, mechanistic investigation, and clinical application.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM058833-11
Application #
7569487
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Schwab, John M
Project Start
1999-02-01
Project End
2010-07-31
Budget Start
2009-03-01
Budget End
2010-07-31
Support Year
11
Fiscal Year
2009
Total Cost
$395,197
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
Karimov, Rashad R; Tan, Derek S; Gin, David Y (2018) Synthesis of the hexacyclic triterpene core of the jujuboside saponins via tandem Wolff rearrangement-intramolecular ketene hetero-Diels-Alder reaction. Tetrahedron 74:3370-3383
Karimov, Rashad R; Tan, Derek S; Gin, David Y (2017) Rapid assembly of the doubly-branched pentasaccharide domain of the immunoadjuvant jujuboside A via convergent B(C6F5)3-catalyzed glycosylation of sterically-hindered precursors. Chem Commun (Camb) 53:5838-5841
Fernández-Tejada, Alberto; Walkowicz, William E; Tan, Derek S et al. (2017) Semisynthesis of Analogues of the Saponin Immunoadjuvant QS-21. Methods Mol Biol 1494:45-71
Fernández-Tejada, Alberto; Tan, Derek S; Gin, David Y (2016) Development of Improved Vaccine Adjuvants Based on the Saponin Natural Product QS-21 through Chemical Synthesis. Acc Chem Res 49:1741-56
Walkowicz, William E; Fernández-Tejada, Alberto; George, Constantine et al. (2016) Quillaja Saponin Variants with Central Glycosidic Linkage Modifications Exhibit Distinct Conformations and Adjuvant Activities. Chem Sci 7:2371-2380
Blazekovic, Francesca; Odukoya, Dana; Butler, Shanitra N et al. (2016) HLA-DR peptide occupancy can be regulated with a wide variety of small molecules. Hum Vaccin Immunother 12:593-8
Fernández-Tejada, Alberto; Tan, Derek S; Gin, David Y (2015) Versatile strategy for the divergent synthesis of linear oligosaccharide domain variants of Quillaja saponin vaccine adjuvants. Chem Commun (Camb) 51:13949-52
Fernández-Tejada, Alberto; Chea, Eric K; George, Constantine et al. (2014) Design, synthesis, and immunologic evaluation of vaccine adjuvant conjugates based on QS-21 and tucaresol. Bioorg Med Chem 22:5917-23
Fernández-Tejada, Alberto; Chea, Eric K; George, Constantine et al. (2014) Development of a minimal saponin vaccine adjuvant based on QS-21. Nat Chem 6:635-43
Chea, Eric K; Fernández-Tejada, Alberto; Damani, Payal et al. (2012) Synthesis and preclinical evaluation of QS-21 variants leading to simplified vaccine adjuvants and mechanistic probes. J Am Chem Soc 134:13448-57

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