Design of a PEGylated Antimicrobial Prodrug with Species-Specific Activation.
Meghan K O'LearySabrina S ChenLars F WestbladeChristopher A AlabiPublished in: Biomacromolecules (2021)
The rise of multidrug-resistant (MDR) "superbugs" has created an urgent need to develop new classes of antimicrobial agents to target these organisms. Oligothioetheramides (oligoTEAs) are a unique class of antimicrobial peptide (AMP) mimetics with one promising compound, BDT-4G, displaying potent activity against MDR Pseudomonas aeruginosa clinical isolates. Despite widely demonstrated potency, BDT-4G and other AMP mimetics have yet to enjoy broad preclinical success against systemic infections, primarily due to their cytotoxicity. In this work, we explore a prodrug strategy to render BDT-4G inactive until it is exposed to an enzyme secreted by the targeted bacteria. The prodrug consists of polyethylene glycol (PEG) conjugated to BDT-4G by a peptide substrate. PEG serves to inactivate and reduce the toxicity of BDT-4G by masking its cationic charge and antimicrobial activity is recovered following site-specific cleavage of the short peptide linker by LasA, a virulence factor secreted by P. aeruginosa. This approach concurrently reduces cytotoxicity by greater than 1 order of magnitude in vitro and provides species specificity through the identity of the cleavable linker.
Keyphrases
- multidrug resistant
- cancer therapy
- pseudomonas aeruginosa
- gram negative
- drug delivery
- staphylococcus aureus
- acinetobacter baumannii
- drug resistant
- drug release
- protein kinase
- biofilm formation
- cystic fibrosis
- escherichia coli
- klebsiella pneumoniae
- oxidative stress
- photodynamic therapy
- stem cells
- cell therapy
- dna binding
- bone marrow