Proline Hinged Amphipathic α‑Helical Peptide Sensitizes Gram-Negative Bacteria to Various Gram-Positive Antibiotics

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...

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Veröffentlicht in:Journal of medicinal chemistry 2020-12, Vol.63 (23), p.14937-14950
Hauptverfasser: Hyun, Soonsil, Choi, Yoonhwa, Jo, Doyeon, Choo, Seolah, Park, Tae Woo, Park, Su-Jin, Kim, Seoyeon, Lee, Seonju, Park, Sohyun, Jin, Sun Mi, Cheon, Dae Hee, Yoo, Wanki, Arya, Rekha, Chong, Yong Pil, Kim, Kyeong Kyu, Kim, Yang Soo, Lee, Yan, Yu, Jaehoon
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Sprache:eng
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Zusammenfassung: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.
ISSN:0022-2623
1520-4804
DOI:10.1021/acs.jmedchem.0c01506