Antimicrobial Agents 2012
DOI: 10.5772/33293
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Natural Antimicrobial Peptides from Eukaryotic Organisms

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Cited by 4 publications
(6 citation statements)
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“…When the threshold concentration level of peptide reaches to maximum, these molecules penetrate into lipid membrane of bacteria. In the year 1999, according to Shai-Matsuzaki-Huang, in ''carpet'' model globular bilayer destabilization occurs which marks the membrane disruption of microorganisms (Conde et al 2012;Berglund et al 2015). …”
Section: Carpet Modelmentioning
confidence: 99%
“…When the threshold concentration level of peptide reaches to maximum, these molecules penetrate into lipid membrane of bacteria. In the year 1999, according to Shai-Matsuzaki-Huang, in ''carpet'' model globular bilayer destabilization occurs which marks the membrane disruption of microorganisms (Conde et al 2012;Berglund et al 2015). …”
Section: Carpet Modelmentioning
confidence: 99%
“…Some examples of peptides that work through the barrel stave model mechanisms are alamethicin and gramicidin S [13,44,45]. Bioinformatic analysis of protegrin 1 conformed that the calculated energy of peptide insertion in artificial membranes was most congruent with this model (Figure 4(a)) [26,33].…”
Section: Barrel-stave Modelmentioning
confidence: 84%
“…AMPs not only directly target and destroy bacteria but may exert their antimicrobial activity by immune modulatory mechanism [20]. AMPs display their immune-modulatory effects in different ways, like reducing the endotoxin-induced inflammatory response, provoking synthesis of pro-inflammatory factors and cytokines, controlling adaptive immunity, and finally recruiting macrophages to show immune modulatory effects [25][26][27]. These peptides enhance the body's ability to fight microbes rather than directly killing bacteria [4].…”
Section: Immunological Regulation Mechanism Of Actionmentioning
confidence: 99%
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“…However, only two types of PTMs are found ubiquitously among the AMPs of eukaryotic organisms [6] of which the first is the oxidation of an amino acid residue (cysteine) to form disulfide bridges [14]. Scientists have observed that disulfide bridges play an important and major architectural role in the antimicrobial effect of AMPs [6], mainly by maintaining the amphipathic topography of the biologically studied molecules and thus their ability to interact with target membranes and kill Host cells [5,15]. This form of structural stabilization is critical for the therapeutic development of AMPs and furthermore is demonstrated by the cysteine knot architectures of cyclotides from plants [2,16].…”
Section: Introductionmentioning
confidence: 99%