Abstract
In our efforts to develop peptide dendrimers as a new
class of antimicrobial peptides (AMPs) against Gram-negative bacteria, we
investigated their activity at acidic and basic pH, which correspond to the
conditions of the site of bacterial infections on skin or biofilms and chronic
wounds respectively. Removing the eight low pKa amino termini
of our reference dendrimer G3KL by substituting the N-terminal
lysine residues with aminohexanoic acid provided dendrimer XC1 with a
broader pH-activity range. Furthermore, raising the pH to 8.0 revealed strong
activities against Klebsiella pneumoniae and methicillin resistant Staphylococcus
aureus (MRSA) against which the dendrimers are inactive at pH 7.4, an
effect which we also observed with polymyxin B and tentatively assign to
stronger binding to the bacteria at higher pH as observed with a fluorescence
labeled dendrimer analog.