This is a match-making section for OHAMR Call for proposals 2026.
H - Human Health
Antimicrobial Peptides ESKAPE Multi-Drug Resistance Protease-Resistant Peptides Membrane-Targeting Therapeutics
While our current university consortium covers peptide synthesis, modification, physicochemical characterization and initial toxicity profiling, along with a partner dedicated to membrane permeability kinetics, we are seeking a strategic partner to complete the validation pipeline. Specifically, we are looking for a partners who have: Partner Profile 1: • Access to a comprehensive biobank of WHO-critical priority Multi-Drug Resistant (MDR) clinical strains (specifically ESKAPE pathogens). • Ability to conduct advanced antimicrobial susceptibility testing on these diverse isolates. • Capacity to validate the efficacy of the peptide library against clinically relevant resistant pathogens to ensure translational relevance. • Contribution to completing the validation pipeline to ensure the translational success of the novel therapeutics Partner Profile 2: • Infrastructure and expertise to establish in vivo animal infection models. • Capability to evaluate the therapeutic efficacy, safety and pharmacokinetics of optimised peptides in living systems. • Contribution to the completion of the validation pipeline, bridging the gap between in vitro results and clinical application and ensuring the translational success of novel therapeutics.
In response to the urgent global challenge of antimicrobial resistance (AMR), our research group has focused on designing and developing bio-inspired antimicrobial peptides. Through extensive screening, we identified a lead candidate, D-TN6, which demonstrates exceptional broad-spectrum activity against both Gram-positive and Gram-negative bacteria, as well as significant antifungal efficacy. Our unpublished data show high potency against roughly 200 multidrug-resistant clinical isolates, particularly the critical ESKAPE pathogens. Within the OHAMR framework, our goal is to further enhance peptide stability in human blood, extend its biological half-life, and optimize its therapeutic index through rational design and modification. Related articles: • Kocagoz, T., Temur, B. Z., Unubol, N., Elmas, M. A., Kanlidere, Z., Cilingir, S., Acar, D., Boskan, G., Deveci, S. A., Aybakan, E., Yoner, A. O., Uyar, N. Y., Serteser, M., Sahsuvar, S., Erdemgil, Y., Keles, Z. Z. Y., Demirhan, D., Sakalauskaite, S., Daugelavicius, R., . . . Can, O. (2025). Protease-Resistant, Broad-Spectrum Antimicrobial Peptides with High Antibacterial and Antifungal Activity. Life, 15(2), 242. https://doi.org/10.3390/life15020242 • Sahsuvar, S., Kocagoz, T., Gok, O., & Can, O. (2023). In vitro efficacy of different PEGylation designs on cathelicidin-like peptide with high antibacterial and antifungal activity. Scientific Reports, 13(1), 11213. https://doi.org/10.1038/s41598-023-38449-3
Submitted on 2025-12-11 08:11:23
« Return to the partner search tool