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- Title
Visualizing the membrane disruption action of antimicrobial peptides by cryo-electron tomography.
- Authors
Chen, Eric H.-L.; Wang, Chun-Hsiung; Liao, Yi-Ting; Chan, Feng-Yueh; Kanaoka, Yui; Uchihashi, Takayuki; Kato, Koichi; Lai, Longsheng; Chang, Yi-Wei; Ho, Meng-Chiao; Chen, Rita P.-Y.
- Abstract
The abuse of antibiotics has led to the emergence of multidrug-resistant microbial pathogens, presenting a pressing challenge in global healthcare. Membrane-disrupting antimicrobial peptides (AMPs) combat so-called superbugs via mechanisms different than conventional antibiotics and have good application prospects in medicine, agriculture, and the food industry. However, the mechanism-of-action of AMPs has not been fully characterized at the cellular level due to a lack of high-resolution imaging technologies that can capture cellular-membrane disruption events in the hydrated state. Previously, we reported PepD2M, a de novo-designed AMP with potent and wide-spectrum bactericidal and fungicidal activity. In this study, we use cryo-electron tomography (cryo-ET) and high-speed atomic force microscopy (HS-AFM) to directly visualize the pepD2M-induced disruption of the outer and inner membranes of the Gram-negative bacterium Escherichia coli, and compared with a well-known pore-forming peptide, melittin. Our high-resolution cryo-ET images reveal how pepD2M disrupts the E. coli membrane using a carpet/detergent-like mechanism. Our studies reveal the direct membrane-disrupting consequence of AMPs on the bacterial membrane by cryo-ET, and this information provides critical insights into the mechanisms of this class of antimicrobial agents. Antimicrobial peptide mechanism of membrane disruption have not been fully characterized at the cellular level. Here, authors use cryo-electron tomography and AFM to directly visualize the disruption of the outer and inner membranes of Escherichia coli by a de novo-designed peptide.
- Subjects
ANTIMICROBIAL peptides; MELITTIN; BACTERIAL cell walls; TOMOGRAPHY; ESCHERICHIA coli; ATOMIC force microscopy; PEPTIDE antibiotics; BACTERICIDAL action
- Publication
Nature Communications, 2023, Vol 14, Issue 1, p1
- ISSN
2041-1723
- Publication type
Article
- DOI
10.1038/s41467-023-41156-2