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Cited by 367

The DOI matches its Crossref record; 91 of the 91 references it cites were found in a registry or an index.

Mode-of-Action of Antimicrobial Peptides: Membrane Disruption vs. Intracellular Mechanisms

Open access
Benfield, Aurélie H., Henriques, Sónia Troeira·2020·Frontiers in Medical Technology

Abstract

Antimicrobial peptides are an attractive alternative to traditional antibiotics, due to their physicochemical properties, activity toward a broad spectrum of bacteria, and mode-of-actions distinct from those used by current antibiotics. In general, antimicrobial peptides kill bacteria by either disrupting their membrane, or by entering inside bacterial cells to interact with intracellular components. Characterization of their mode-of-action is essential to improve their activity, avoid resistance in bacterial pathogens, and accelerate their use as therapeutics. Here we review experimental biophysical tools that can be employed with model membranes and bacterial cells to characterize the mode-of-action of antimicrobial peptides.

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Crossref · 10.3389/fmedt.2020.610997

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Metadata

Authors
Benfield, A. H., & Henriques, S. T.
Venue
Frontiers in Medical Technology
Published
2020-12-11
Volume
2
Pages
610997-610997
ISSN
2673-3129 (ISSN-L)
OpenAlex
W3111531342
Cited by
367
References
91
FWCI
17.82
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Mode-of-Action of Antimicrobial Peptides: Membrane Disruption vs. Intracellular Mechanisms. https://app.cochat.ai/papers/10.3389/fmedt.2020.610997
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Benfield, A. H., & Henriques, S. T. (2020). Mode-of-Action of Antimicrobial Peptides: Membrane Disruption vs. Intracellular Mechanisms. Frontiers in Medical Technology. https://doi.org/10.3389/fmedt.2020.610997

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.