<?xml version="1.0"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=175081"><dc:title>AI-guided design of new antimicrobial peptides</dc:title><dc:creator>Milova,	Evgeniia	(Avtor)
	</dc:creator><dc:creator>Podlipnik,	Črtomir	(Mentor)
	</dc:creator><dc:subject>antimicrobial peptides</dc:subject><dc:subject>explainable artificial intelligence</dc:subject><dc:subject>generative topographic mapping</dc:subject><dc:subject>Wasserstein autoencoder</dc:subject><dc:description>Antimicrobial resistance (AMR) is a growing threat to global health, driven by the
overuse of antibiotics and the lack of novel therapeutic agents. Antimicrobial peptides
(AMPs) have emerged as promising alternative to traditional small molecule-based
antibiotics due to their broad-spectrum activity and reduced susceptibility to resistance.
Recent advances in generative deep learning provided new tools for the design of AMPs
allowing rationalization and speeding up the process of their development. While
showing efficacy in generating AMPs, such methods often lack interpretability required
to efficient used by domain experts. In this study, we build upon a previously established
workflow that combines a Wasserstein Autoencoder (WAE) with Generative
Topographic Mapping (GTM) — a visualization technique that enables an interpretable
sampling from the latent space. The method was applied for the design of AMPs against
Staphylococcus aureus, achieving a high experimental hit rate. However, the original
method was limited to in-house data on anti-S. aureus peptides containing 10 to 14
residues. In this work, the approach was extended to 14 bacterial species and 15 bacterial
strains, using peptide sequences with an extended range of lengths (6-25 amino acid
residues). In addition to that, various sequence representation methods, including 2-mers,
3-mers, protein large language model (pLLM) were investigated. The extended workflow
enables to identify the zones associated with broad-spectrum antimicrobial activity on
GTM landscapes and to guide targeted sampling from these zones. For in silico
predictions of peptides activity, Support Vector Machine (SVM), CatBoost and Random
Forest (RF) machine learning models were used. Based on the activity predictions, 10
peptides were selected and validated in vitro by a partner laboratory. In total 5 out of 10
peptides possessed at least 1 activity: 3 of these peptides were active against
Staphylococcus epidermidis, and 2 of them showed broad-spectrum antimicrobial activity
against S. epidermidis and S. aureus. This approach has demonstrated the potential of this
interpretable generative framework for the discovery of broad-spectrum AMPs.</dc:description><dc:date>2025</dc:date><dc:date>2025-10-15 09:05:01</dc:date><dc:type>Magistrsko delo/naloga</dc:type><dc:identifier>175081</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
