2018
DOI: 10.1016/j.bbamem.2018.10.003
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Effects of the peptide Magainin H2 on Supported Lipid Bilayers studied by different biophysical techniques

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Cited by 16 publications
(18 citation statements)
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“…First, the lateral expansion of the membrane induced by the interaction with the AMP is inhibited. Further, it proceeds to create new bilayer regions with many defects in the membrane [ 79 , 80 ].…”
Section: Resultsmentioning
confidence: 99%
“…First, the lateral expansion of the membrane induced by the interaction with the AMP is inhibited. Further, it proceeds to create new bilayer regions with many defects in the membrane [ 79 , 80 ].…”
Section: Resultsmentioning
confidence: 99%
“…For peptide-bound membranes a much lower force is needed to puncture through the bilayer. [89,97,101,102] In some cases, destabilisation of the membrane occurs at very low peptide concentrations. [97] In other cases a threshold peptide concentration is needed, below which peptide addition increases the force needed to puncture the membrane, presumably because peptide binding to the membrane surface increases the lateral pressure at the surface.…”
Section: Mechanical Destabilisationmentioning
confidence: 99%
“…[97] In other cases a threshold peptide concentration is needed, below which peptide addition increases the force needed to puncture the membrane, presumably because peptide binding to the membrane surface increases the lateral pressure at the surface. [101,102] To date, there have been few studies comparing the relationship between bilayer stability and topographical defects formed. In one, the extent of destabilisation correlated with the number of nanoscale pits was observed.…”
Section: Mechanical Destabilisationmentioning
confidence: 99%
“…Several ways of exploiting the AMPs properties, such as Magainin H2, have a high level of hydrophobicity and present a good permeabilization action on lipid bilayers. Thus, experimental and theoretical studies investigated how AMPs and lipid bilayers interact, concluding that, at first, the lateral growth of the membrane caused by interactions with the AMP is inhibited, but in the end, it generates new bilayer regions that have defects in their membrane [69,70]. Another feasible option is the combined use of AMPs and conventional antibiotics, showing synergy and lowering microbial resistance [71].…”
Section: Antimicrobial Agents and Antimicrobial Resistancementioning
confidence: 99%