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Proline Hinged Amphipathic α-Helical Peptide Sensitizes Gram-Negative Bacteria to Various Gram-Positive Antibiotics
- Source :
- Journal of Medicinal Chemistry. 63:14937-14950
- Publication Year :
- 2020
- Publisher :
- American Chemical Society (ACS), 2020.
-
Abstract
- Gram-negative bacteria are becoming resistant to almost all currently available antibiotics. Systemically designed antimicrobial peptides (AMPs) are attractive agents to enhance the activities of antibiotics. We constructed a small Pro-scanning library using amphipathic model peptides. Measurements of minimum inhibitory concentration (MIC) against Escherichia coli and hemolytic activities showed that one of the Pro-hinged peptides, KL-L9P, displays the highest specificity toward E. coli. Moreover, KL-L9P sensitizes E. coli to be responsive to most antibiotics that are not active against Gram-negative bacteria. The results of biochemical experiments show that KL-L9P promotes the rearrangement of the bacterial membrane that enables hydrophobic antibiotics to permeate. Finally, the results of animal tests demonstrate that KL-L9P strongly sensitizes Gram-negative bacteria to linezolid (Lzd), rifampicin (Rif), or clarithromycin (Clr). Thus, KL-L9P operates as a sensitizer to extend the antibacterial activity of most antibiotics to Gram-negative bacteria.
- Subjects :
- Protein Conformation, alpha-Helical
Gram-negative bacteria
Proline
Membrane Fluidity
medicine.drug_class
Antibiotics
Antimicrobial peptides
Microbial Sensitivity Tests
medicine.disease_cause
Hemolysis
01 natural sciences
Microbiology
03 medical and health sciences
chemistry.chemical_compound
Minimum inhibitory concentration
Clarithromycin
Drug Discovery
Escherichia coli
medicine
Animals
Humans
030304 developmental biology
Mice, Inbred ICR
0303 health sciences
biology
Chemistry
Cell Membrane
Linezolid
biology.organism_classification
Anti-Bacterial Agents
0104 chemical sciences
010404 medicinal & biomolecular chemistry
Lipid A
Molecular Medicine
Female
Rifampin
Antibacterial activity
Hydrophobic and Hydrophilic Interactions
Bacteria
Antimicrobial Cationic Peptides
Protein Binding
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 63
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....22d10a9a9f80fd0c3b72cba4db098f99