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<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://dk.um.si/IzpisGradiva.php?id=65459"><dc:title>Effect of peptides' binding on the antimicrobial activity and biocompatibility of ‎protein-based substrates ‎</dc:title><dc:creator>Kaisersberger Vincek,	Maja	(Avtor)
	</dc:creator><dc:creator>Kokol,	Vanja	(Mentor)
	</dc:creator><dc:subject>wool</dc:subject><dc:subject>gelatine</dc:subject><dc:subject>antimicrobial peptides</dc:subject><dc:subject>ε-poly-L-lysine</dc:subject><dc:subject>oligo-acyl-lysyl</dc:subject><dc:subject>grafting chemistry</dc:subject><dc:subject>‎grafting approach</dc:subject><dc:subject>peptide orientation</dc:subject><dc:subject>antibacterial activity</dc:subject><dc:subject>cytotoxicity‎</dc:subject><dc:description>This work reveals the effect of coupling approach (chemical by using carbodiimide chemistry ‎and grafting-to vs. grafting-from synthesis routes, and enzymatic by using transglutaminase) ‎of a hydrophilic ε-poly-L-lysine (εPL) and an amphiphilic oligo-acyl-lysyl (OAK) derivative (K-7α12-OH) to wool fibers and gelatine (GEL) macromolecules, respectively, and substrates ‎antibacterial activity against Gram-negative E. coli and Gram-positive S. aureus bacteria ‎after 1–24 h of exposure, as well as their cytotoxicity. Different spectroscopic (ultraviolet-‎visible, infrared, fluorescence and electron paramagnetic resonance) and separation ‎techniques (size-exclusion chromatography and capillary zone electrophoresis) as well as ‎zeta potential and potentiometric titration analysis, were performed to confirm the covalent ‎coupling of εPL/OAK, and to determine the amount and orientation of its immobilisation.‎
The highest and kinetically the fastest level of bacterial reduction was achieved with ‎wool/GEL functionalised with εPL/OAK by chemical grafting-to approach. This effect ‎correlated with both the highest grafting yield and conformationally the highly-flexible ‎(brush-like) orientation linkage of εPL/OAK, implicating on the highest amount of accessible ‎amino groups interacting with bacterial membrane. However, OAK`s amphipathic structure, ‎the cationic charge and the hydrophobic moieties, resulted to relatively high reduction of S. ‎aureus for grafting-from and the enzymatic coupling approaches using OAK-functionalised ‎GEL. ‎
The εPL/OAK-functionalised GEL did not induce toxicity in human osteoblast cells, even at ‎‎~25-fold higher concentration than bacterial minimum inhibitory (MIC) concentration of ‎εPL/OAK, supporting their potential usage in biomedical applications.‎
It was also shown that non-ionic surfactant adsorbs strongly onto the wool surface during ‎the process of washing, thereby blocking the functional sites of immobilized εPL and ‎decreases its antibacterial efficiency. ‎
‎</dc:description><dc:publisher>[M. Kaisersberger Vincek]</dc:publisher><dc:date>2017</dc:date><dc:date>2017-04-05 20:16:33</dc:date><dc:type>Doktorska disertacija</dc:type><dc:identifier>65459</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
