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 residues used in the amino acid sequence of the AMPs under investigation.</div>

International Journal of Medicinal Chemistry

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Figure 1

Figure 1: Synthetic Antimicrobial Peptides Exhibit Two Different Binding Mechanisms to the Lipopolysaccharides Isolated from <i>Pseudomonas aeruginosa</i> and <i>Klebsiella pneumoniae</i> 

Figure 1 | Synthetic Antimicrobial Peptides Exhibit Two Different Binding Mechanisms to the Lipopolysaccharides Isolated from Pseudomonas aeruginosa and Klebsiella pneumoniae 