Date of Award
Spring 5-15-2026
Degree Type
Dissertation
Degree Name
PhD. Chemistry
Department
Chemistry and Biochemistry
Advisor
Gregory R. Wiedman, Ph.D.
Committee Member
Wyatt R. Murphy, Ph.D.
Committee Member
Nicholas H. Snow, Ph.D.
Keywords
antifungal peptides, Candida auris, reactive oxygen species, ATCUN
Abstract
A recently emerged opportunistic fungi, Candida auris, has been subject to increased scrutiny due to its virulence and rapid geographical spread. Due to the indiscriminate use of antimicrobials as treatments for infectious diseases and as pesticides, the ubiquitous threat of multidrug resistance (MDR) looms large. The lack of progress in antifungal development is of high concern in the treatment of infectious diseases and a rise in fungal resistance highlight the need for updated treatment strategies. This work describes three strategies used to address these concerns:
- The synthesis of a photosensitizer-membrane-active peptide (PS-MAP) conjugate, Ir-HKII15, that combines the ability of photosensitizers to produce membrane-damaging reactive oxygen species (ROS) with the destabilizing effects associated with membrane-active peptides (MAPs);
- The design of a combinatorial peptide library that incorporates the well-studied ATCUN (amino terminal copper and nickel) binding motif into a translocating peptide sequence, TP2; and
- Combining the benefits of rational design and combinatorial libraries while avoiding the limitations of introducing single amino acid modifications and allows for direct microbiological testing.
Recommended Citation
Mateen, Akilah I., "Semi-rational Strategies for Antifungal Peptide Design" (2026). Seton Hall University Dissertations and Theses (ETDs). 4467.
https://scholarship.shu.edu/dissertations/4467