Complex carbohydrates are involved in a broad variety of biological phenomena and their involvement in disease processes, in particular, have given this class of natural compounds a tremendous diagnostic and therapeutic potential. To this end, the PI's and co-PI's laboratories have focused their research efforts towards carbohydrates associated with diseases that rank among the top 10 leading causes of death worldwide, i.e. cancer, pneumococcal disease, septicemia, and Alzheimer's disease. At the core of this effort is the belief that if a comprehensive knowledge of the structure, conformation, and properties of these carbohydrates were available, elucidation of the mechanisms for the pathogenesis of these diseases could be facilitated. Consequently, this could lead to the development of effective tools for the prevention, diagnosis, and/or treatment of these diseases. The long-term goals of the PI's and co-PI's research programs are to make complex carbohydrates more accessible to general chemical, biochemical, medical and industrial audiences, and thereby keep pace with the exploding areas of glycobiology and related health sciences. Proposed herein is the expansion of studies initiated in our laboratories for the development of novel high-throughput technologies for oligosaccharide and glycoconjugate synthesis. At the core of this proposal is the development of a new strategy for supported synthesis called STICS (Surface-Tethered Iterative Carbohydrate Synthesis). The intellectual merit of the proposed research lies in its significant contributions to the field of basic and applied synthetic carbohydrate, surface, and nanomaterial chemistries upon its successful completion. Precisely, the success of this endeavor will not only advance the field of chemistries mentioned, but also fundamentally contribute to further development of glyco- and nanotechnology in general. We trust that the proposed developments will lead to the discovery of novel methodologies for the efficient synthesis and high throughput screening of carbohydrate-based libraries and therapeutics. A broader and long-term impact of this work relate to the professional training in surface, preparative organic, carbohydrate, bioorganic, and materials chemistry that undergraduate, graduate and post-doctoral research participants will receive. In addition, the multidisciplinary nature of the proposed research will allow students to expand their scientific base in an intellectual and practical sense. During their laboratory experience they will learn important tools that allow obtain, modify, and analyze organic molecules and nanomaterials by means of developing new methodologies and participating in the elaboration of state-of-the-art, multi-step syntheses. Student researchers will also become integrated into the scientific community through the preparation of manuscripts and attendance at professional meetings. As a consequence, students will develop better communication skills while also being exposed to scientific discourse. Finally, the proposed research will ultimately strengthen interdisciplinary collaborations with biomedical researchers.

Public Health Relevance

The proposed research will benefit human health by developing a new strategy for synthesizing carbohydrates significant in diagnosing and treating diseases including cancer and autoimmune diseases, and in the development of new therapies based on stem cells. The new technology for surface supported carbohydrate synthesis will result in these molecules becoming more accessible for biological studies that can lead to development of therapeutic agents. The nanomaterials used for our new approach to supported syntheses can also be used for diagnostic assays and stem cell biology sorting applications using the carbohydrates made as a part of this project.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM090254-02
Application #
7939800
Study Section
Special Emphasis Panel (ZGM1-PPBC-3 (CS))
Program Officer
Marino, Pamela
Project Start
2009-09-30
Project End
2013-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
2
Fiscal Year
2010
Total Cost
$261,608
Indirect Cost
Name
University of Missouri-St. Louis
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
804883825
City
Saint Louis
State
MO
Country
United States
Zip Code
63121
Bhattarai, Jay K; Neupane, Dharmendra; Nepal, Bishal et al. (2018) Preparation, Modification, Characterization, and Biosensing Application of Nanoporous Gold Using Electrochemical Techniques. Nanomaterials (Basel) 8:
Bhattarai, Jay K; Tan, Yih Horng; Pandey, Binod et al. (2016) Electrochemical Impedance Spectroscopy Study of Concanavalin A Binding to Self-Assembled Monolayers of Mannosides on Gold Wire Electrodes. J Electroanal Chem (Lausanne) 780:311-320
Sharma, Abeera; Bhattarai, Jay K; Nigudkar, Swati S et al. (2016) Electrochemical impedance spectroscopy study of carbohydrate-terminated alkanethiol monolayers on nanoporous gold: Implications for pore wetting. J Electroanal Chem (Lausanne) 782:174-181
Bhattarai, Jay K; Sharma, Abeera; Fujikawa, Kohki et al. (2015) Electrochemical synthesis of nanostructured gold film for the study of carbohydrate-lectin interactions using localized surface plasmon resonance spectroscopy. Carbohydr Res 405:55-65
Sharma, Abeera; Bhattarai, Jay K; Alla, Allan J et al. (2015) Electrochemical annealing of nanoporous gold by application of cyclic potential sweeps. Nanotechnology 26:085602
Alla, Allan J; D' Andrea, Felipe B; Bhattarai, Jay K et al. (2015) Selective capture of glycoproteins using lectin-modified nanoporous gold monolith. J Chromatogr A 1423:19-30
Pandey, Binod; Bhattarai, Jay K; Pornsuriyasak, Papapida et al. (2014) Square-wave voltammetry assays for glycoproteins on nanoporous gold. J Electroanal Chem (Lausanne) 717-718:47-60
Nigudkar, Swati S; Stine, Keith J; Demchenko, Alexei V (2014) Regenerative glycosylation under nucleophilic catalysis. J Am Chem Soc 136:921-3
Nigudkar, Swati S; Parameswar, Archana R; Pornsuriyasak, Papapida et al. (2013) O-Benzoxazolyl imidates as versatile glycosyl donors for chemical glycosylation. Org Biomol Chem 11:4068-76
Ganesh, N Vijaya; Fujikawa, Kohki; Tan, Yih Horng et al. (2013) Surface-tethered iterative carbohydrate synthesis: a spacer study. J Org Chem 78:6849-57

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