Literature DB >> 27410741

Mode of Action of Antimicrobial Peptides on E. coli Spheroplasts.

Yen Sun1, Tzu-Lin Sun1, Huey W Huang2.   

Abstract

We investigated the phenomena of antimicrobial peptides (AMPs) directly attacking the cytoplasmic membranes of Escherichia coli spheroplasts. We developed a procedure for fluorescence recovery after photobleaching to examine dye leakage through bacterial membranes as AMPs in solution bound to the membranes. We found that the AMP binding did not increase the apparent membrane area of a spheroplast, contrary to the response of a lipid-bilayer vesicle, which always showed a membrane area expansion by AMP binding. The permeability through the bacterial membrane increased in a sigmoidal fashion as the AMP binding increased in time, exhibiting a cooperative behavior of AMPs. The analysis of fluorescence recovery after photobleaching showed that the fluxes of dye molecules into and out of the cell were consistent with diffusion of molecules through a number of pores that increased with binding of AMPs and then saturated to a steady level. We discovered a new, to our knowledge, experimental parameter called the flux rate that characterizes the AMP-induced permeability of dye molecules through bacterial membranes. The phenomena observed in bacterial membranes are consistent with the pore-forming activities of AMPs previously observed in lipid bilayers. The experimental value of the flux rate per pore is much smaller than a theoretical value that assumes no friction for the dye molecule's permeation through the pore. We believe that experimental studies of the flux rate will be useful for further analysis of AMPs' permeabilization mechanisms.
Copyright © 2016 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27410741      PMCID: PMC4944488          DOI: 10.1016/j.bpj.2016.05.037

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  32 in total

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3.  High-affinity fluorescent peptide binding to I-Ad in lipid membranes.

Authors:  T H Watts; H M McConnell
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Review 4.  Bactericidal/permeability increasing protein and host defense against gram-negative bacteria and endotoxin.

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5.  Activities of LL-37, a cathelin-associated antimicrobial peptide of human neutrophils.

Authors:  J Turner; Y Cho; N N Dinh; A J Waring; R I Lehrer
Journal:  Antimicrob Agents Chemother       Date:  1998-09       Impact factor: 5.191

6.  All-D amino acid-containing channel-forming antibiotic peptides.

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Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

7.  Binding of LL-37 to model biomembranes: insight into target vs host cell recognition.

Authors:  Rohit Sood; Yegor Domanov; Milla Pietiäinen; Vesa P Kontinen; Paavo K J Kinnunen
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8.  NMR structure of the cathelicidin-derived human antimicrobial peptide LL-37 in dodecylphosphocholine micelles.

Authors:  Fernando Porcelli; Raffaello Verardi; Lei Shi; Katherine A Henzler-Wildman; Ayyalusamy Ramamoorthy; Gianluigi Veglia
Journal:  Biochemistry       Date:  2008-04-26       Impact factor: 3.162

9.  Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor.

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Authors:  G Bierbaum; H G Sahl
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  11 in total

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2.  Molecular State of the Membrane-Active Antibiotic Daptomycin.

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5.  Using fluorescence microscopy to shed light on the mechanisms of antimicrobial peptides.

Authors:  Anne K Buck; Donald E Elmore; Louise Eo Darling
Journal:  Future Med Chem       Date:  2019-09-13       Impact factor: 3.808

Review 6.  Role of Lipid Composition, Physicochemical Interactions, and Membrane Mechanics in the Molecular Actions of Microbial Cyclic Lipopeptides.

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7.  Production and Visualization of Bacterial Spheroplasts and Protoplasts to Characterize Antimicrobial Peptide Localization.

Authors:  Dania M Figueroa; Heidi M Wade; Katrina P Montales; Donald E Elmore; Louise E O Darling
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Review 8.  Action of antimicrobial peptides and cell-penetrating peptides on membrane potential revealed by the single GUV method.

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Journal:  Biophys Rev       Date:  2020-03-09

9.  In vivo analysis of the Escherichia coli ultrastructure by small-angle scattering.

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10.  Regulation of Antimicrobial Peptide Activity via Tuning Deformation Fields by Membrane-Deforming Inclusions.

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