<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bluhm ME</submitter><funding>Bundesministerium für Bildung und Forschung</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Sächsische Aufbaubank</funding><pagination>39</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4861708</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4</volume><pubmed_abstract>The Gram-negative bacterium Pseudomonas aeruginosa is a life-threatening nosocomial pathogen due to its generally low susceptibility toward antibiotics. Furthermore, many strains have acquired resistance mechanisms requiring new antimicrobials with novel mechanisms to enhance treatment options. Proline-rich antimicrobial peptides, such as the apidaecin analog Api137, are highly efficient against various Enterobacteriaceae infections in mice, but less active against P. aeruginosa in vitro. Here, we extended our recent work by optimizing lead peptides Api755 (gu-OIORPVYOPRPRPPHPRL-OH; gu = N,N,N',N'-tetramethylguanidino, O = L-ornithine) and Api760 (gu-OWORPVYOPRPRPPHPRL-OH) by incorporation of Ile-Orn- and Trp-Orn-motifs, respectively. Api795 (gu-O(IO)2RPVYOPRPRPPHPRL-OH) and Api794 (gu-O(W</pubmed_abstract><journal>Frontiers in cell and developmental biology</journal><pubmed_title>N-Terminal Ile-Orn- and Trp-Orn-Motif Repeats Enhance Membrane Interaction and Increase the Antimicrobial Activity of Apidaecins against Pseudomonas aeruginosa.</pubmed_title><pmcid>PMC4861708</pmcid><funding_grant_id>01GU1104A</funding_grant_id><funding_grant_id>100105139</funding_grant_id><funding_grant_id>100127675</funding_grant_id><pubmed_authors>Schneider VA</pubmed_authors><pubmed_authors>Goldbach T</pubmed_authors><pubmed_authors>Knappe D</pubmed_authors><pubmed_authors>Piantavigna S</pubmed_authors><pubmed_authors>Bluhm ME</pubmed_authors><pubmed_authors>Seibel P</pubmed_authors><pubmed_authors>Schafer I</pubmed_authors><pubmed_authors>Veldhuizen EJ</pubmed_authors><pubmed_authors>Martin LL</pubmed_authors><pubmed_authors>Hoffmann R</pubmed_authors></additional><is_claimable>false</is_claimable><name>N-Terminal Ile-Orn- and Trp-Orn-Motif Repeats Enhance Membrane Interaction and Increase the Antimicrobial Activity of Apidaecins against Pseudomonas aeruginosa.</name><description>The Gram-negative bacterium Pseudomonas aeruginosa is a life-threatening nosocomial pathogen due to its generally low susceptibility toward antibiotics. Furthermore, many strains have acquired resistance mechanisms requiring new antimicrobials with novel mechanisms to enhance treatment options. Proline-rich antimicrobial peptides, such as the apidaecin analog Api137, are highly efficient against various Enterobacteriaceae infections in mice, but less active against P. aeruginosa in vitro. Here, we extended our recent work by optimizing lead peptides Api755 (gu-OIORPVYOPRPRPPHPRL-OH; gu = N,N,N',N'-tetramethylguanidino, O = L-ornithine) and Api760 (gu-OWORPVYOPRPRPPHPRL-OH) by incorporation of Ile-Orn- and Trp-Orn-motifs, respectively. Api795 (gu-O(IO)2RPVYOPRPRPPHPRL-OH) and Api794 (gu-O(W</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2025-06-01T12:23:22.765Z</modification><creation>2025-06-01T12:23:22.765Z</creation></dates><accession>S-EPMC4861708</accession><cross_references><pubmed>27243004</pubmed><doi>10.3389/fcell.2016.00039</doi></cross_references></HashMap>