Mechanisms of Antimicrobial Peptide Action and Resistance
By Michael R. Yeaman, N. Yount. Pharmacological Reviews, 2003
2,925 citations recorded by the source corpus.
Subfields: Emergency Medical Services, Immunology, Microbiology
View Paper: https://www.semanticscholar.org/paper/b2488e5a414bc33d77996977d6cca30be3c04ad6
How researchers see this paper
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In Emergency Medical Services
In Immunology
- Robert E. W. Hancock
- D. Ren
- A. A. Bahar
- H. Jenssen
- Alexandra R. Fernandes
- Prashant Kumar
- Christopher D. Fjell
- Pedro Viana Baptista
In Microbiology
- Robert E. W. Hancock
- D. Ren
- A. A. Bahar
- H. Jenssen
- L. Ringstad
- Joakim Håkansson
- Camilla Björn
- M. Mahlapuu
Citations in the corpus
- Mechanisms of Cellular Uptake of Cell-Penetrating Peptides (2011, methodology): “AMPs also consist of short sequences of cationic and hydrophobic peptides [76, 77].”
- Application of antimicrobial peptides in agriculture and food industry (2009, background): “developing proteolytic activities) strategies ( Yeaman and Yount 2003 ).”
- Antimicrobial peptides: an overview of a promising class of therapeutics (2007, background): “Yet, this peptide is an efficient antimicrobial agent that causes membrane disruption due to a concentrated layer of peptide monomers on the surface [46, 52].”
- CAMP: a useful resource for research on antimicrobial peptides (2009, background): “They generally act on structural components of the cell wall and can have multiple cellular targets (2).”
- Antimicrobial Peptides: An Emerging Category of Therapeutic Agents (2016, background): “The fundamental differences between microbial and mammalian membranes protect mammalian cells against AMPs and enable selective action of these peptides (Yeaman and Yount, 2003).”
- Antimicrobial Peptides (2013, background): “different stages of cell growth [237], and biofilm formation [229].”
- Antimicrobial Peptides: Diversity, Mechanism of Action and Strategies to Improve the Activity and Biocompatibility In Vivo (2018, methodology): “Other features of the toroidal pore include ion selectivity and discrete size [69].”
- From antimicrobial to anticancer peptides. A review (2013, background): “This points to the possibility of the same peptide to act by different mechanisms depending on the cell type in question (Yoo et al., 1997; Eliassen et al., 2006) and to be selective against determined types of cancer.”
- Mechanisms and consequences of bacterial resistance to antimicrobial peptides. (2016, background): “The molecular basis of inducible AMP resistance has been reviewed extensively for both Gram-negative and Gram-positive bacteria (Anaya-Lopez et al., 2013; Gunn, 2001; Kraus and Peschel, 2006; Matamouros and Miller, 2015; Nawrocki et al., 2014; Nizet, 2006; Yeaman and Yount, 2003).”
- Antimicrobial peptides: linking partition, activity and high membrane-bound concentrations (2009, background): “Despite sharing a few common features (for example, cationicity, amphipathicity and short size), AMP sequences vary greatly, and at least four structural groups (α-helical, β-sheet, extended and looped) have been proposed to accommodate the diversity of the observed AMP conformation”
- Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies (2006, background): “Indeed, the action of many peptides cannot be explained by disruption of membrane permeability barriers, as discussed in several review”
- Use of artificial intelligence in the design of small peptide antibiotics effective against a broad spectrum of highly antibiotic-resistant superbugs. (2009, background): “It is important to note that peptides from each quartile had similar charge, hydrophobicity, and amphipathicity/ hydrophobic moment (Figure 2, panels a d), each of which have been considered to be critical determinants for the design of effective antimicrobial peptides (19, 25, 31).”