Synthetic Antimicrobial Peptides Exhibit Two Different Binding Mechanisms to the Lipopolysaccharides Isolated from <i>Pseudomonas aeruginosa</i> and <i>Klebsiella pneumoniae</i>

<div>A representation of the proposed AMP-LPS “active site” which is consistent with the AMP adopting a helical conformation upon binding. Blue semicircles represent anionic sites on LPS. Green semicircles represent hydrophobic binding pockets on LPS.</div>

International Journal of Medicinal Chemistry

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Figure 6

Figure 6: Synthetic Antimicrobial Peptides Exhibit Two Different Binding Mechanisms to the Lipopolysaccharides Isolated from <i>Pseudomonas aeruginosa</i> and <i>Klebsiella pneumoniae</i> 

Figure 6 | Synthetic Antimicrobial Peptides Exhibit Two Different Binding Mechanisms to the Lipopolysaccharides Isolated from Pseudomonas aeruginosa and Klebsiella pneumoniae 