Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/106719
Title: Resurrecting inactive antimicrobial peptides from the lipopolysaccharide trap
Authors: Mohanram, Harini
Bhattacharjya, Surajit
Keywords: DRNTU::Science::Biological sciences::Microbiology
Issue Date: 2014
Source: Mohanram, H., & Bhattacharjya, S. (2014). Resurrecting inactive antimicrobial peptides from the lipopolysaccharide trap. Antimicrobial agents and chemotherapy, 58(4), 1987-1996.
Series/Report no.: Antimicrobial agents and chemotherapy
Abstract: Host defense antimicrobial peptides (AMPs) are a promising source of antibiotics for the treatment of multiple-drug-resistant pathogens. Lipopolysaccharide (LPS), the major component of the outer leaflet of the outer membrane of Gram-negative bacteria, functions as a permeability barrier against a variety of molecules, including AMPs. Further, LPS or endotoxin is the causative agent of sepsis killing 100,000 people per year in the United States alone. LPS can restrict the activity of AMPs inducing aggregations at the outer membrane, as observed for frog AMPs, temporins, and also in model AMPs. Aggregated AMPs, "trapped" by the outer membrane, are unable to traverse the cell wall, causing their inactivation. In this work, we show that these inactive AMPs can overcome LPS-induced aggregations while conjugated with a short LPS binding β-boomerang peptide motif and become highly bactericidal. The generated hybrid peptides exhibit activity against Gram-negative and Gram-positive bacteria in high-salt conditions and detoxify endotoxin. Structural and biophysical studies establish the mechanism of action of these peptides in LPS outer membrane. Most importantly, this study provides a new concept for the development of a potent broad-spectrum antibiotic with efficient outer membrane disruption as the mode of action.
URI: https://hdl.handle.net/10356/106719
http://hdl.handle.net/10220/25116
ISSN: 0066-4804
DOI: 10.1128/AAC.02321-13
Rights: © 2014 American Society for Microbiology. This is the author created version of a work that has been peer reviewed and accepted for publication by Antimicrobial Agents and Chemotherapy, American Society for Microbiology. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1128/AAC.02321-13].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles

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