Biomedical Engineering ETDs
Publication Date
Spring 4-15-2019
Abstract
The goal of this investigation is to study mechanisms the immune cell receptor, Dectin-1, uses to identify the fungal cell species, Candida albicans. Dectin-1 identifies extracellular matrix polysaccharides that Candida albicans express known as β-glucan. To study the interaction of β-glucan – Dectin-1 at the nanoscopic scale, the investigators of this project have endeavored to model the Candida albicans cell wall with engineered Self-Assembled Monolayers presenting β-glucan as a ligand for immobilized Dectin-1 receptors. By engineering a simplified ex-vivo model of the Candida albicans cell wall, the investigators of this study aim to gain precise control of the composition and structure of the delicate embedded nanostructured supra-molecular assemblies that define the cell wall of Candida albicans. The investigator has proposed developing the synthetic model of the cell wall using Self-Assembled Monolayers and Biotin-Streptavidin chemistry to host β-glucan polysaccharides as ligands.
Language
English
Keywords
Candida albicans, Beta-Glucan, Self-Assembled Monolayers, Streptavidin, Biotin
Document Type
Thesis
Degree Name
Biomedical Engineering
Level of Degree
Masters
Department Name
Biomedical Engineering
First Committee Member (Chair)
Aaron Neumann
Second Committee Member
David Whitten
Third Committee Member
Linnea Ista
Recommended Citation
Ghosh, Ushnik. "Developing a synthetic model of the Candida albicans cell wall using Self-Assembled Monolayers to host Beta-glucan as ligands." (2019). https://digitalrepository.unm.edu/bme_etds/23