An Accurate In Vitro Model of the E. coli Envelope

Gram‐negative bacteria are an increasingly serious source of antibiotic‐resistant infections, partly owing to their characteristic protective envelope. This complex, 20 nm thick barrier includes a highly impermeable, asymmetric bilayer outer membrane (OM), which plays a pivotal role in resisting ant...

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Veröffentlicht in:Angewandte Chemie International Edition 2015-10, Vol.54 (41), p.11952-11955
Hauptverfasser: Clifton, Luke A., Holt, Stephen A., Hughes, Arwel V., Daulton, Emma L., Arunmanee, Wanatchaporn, Heinrich, Frank, Khalid, Syma, Jefferies, Damien, Charlton, Timothy R., Webster, John R. P., Kinane, Christian J., Lakey, Jeremy H.
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container_end_page 11955
container_issue 41
container_start_page 11952
container_title Angewandte Chemie International Edition
container_volume 54
creator Clifton, Luke A.
Holt, Stephen A.
Hughes, Arwel V.
Daulton, Emma L.
Arunmanee, Wanatchaporn
Heinrich, Frank
Khalid, Syma
Jefferies, Damien
Charlton, Timothy R.
Webster, John R. P.
Kinane, Christian J.
Lakey, Jeremy H.
description Gram‐negative bacteria are an increasingly serious source of antibiotic‐resistant infections, partly owing to their characteristic protective envelope. This complex, 20 nm thick barrier includes a highly impermeable, asymmetric bilayer outer membrane (OM), which plays a pivotal role in resisting antibacterial chemotherapy. Nevertheless, the OM molecular structure and its dynamics are poorly understood because the structure is difficult to recreate or study in vitro. The successful formation and characterization of a fully asymmetric model envelope using Langmuir–Blodgett and Langmuir–Schaefer methods is now reported. Neutron reflectivity and isotopic labeling confirmed the expected structure and asymmetry and showed that experiments with antibacterial proteins reproduced published in vivo behavior. By closely recreating natural OM behavior, this model provides a much needed robust system for antibiotic development. Understanding the outer membranes of Gram‐negative bacteria is important for the development of new antibacterial compounds. However, their structure and dynamics are poorly understood because of their small in vivo size and inaccurate in vitro models. A stable asymmetric model of the outer membrane that can be analyzed by a range of biophysical techniques and accurately imitates the in vivo behavior of natural outer membranes is presented herein.
doi_str_mv 10.1002/anie.201504287
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Neutron reflectivity and isotopic labeling confirmed the expected structure and asymmetry and showed that experiments with antibacterial proteins reproduced published in vivo behavior. By closely recreating natural OM behavior, this model provides a much needed robust system for antibiotic development. Understanding the outer membranes of Gram‐negative bacteria is important for the development of new antibacterial compounds. However, their structure and dynamics are poorly understood because of their small in vivo size and inaccurate in vitro models. 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Neutron reflectivity and isotopic labeling confirmed the expected structure and asymmetry and showed that experiments with antibacterial proteins reproduced published in vivo behavior. By closely recreating natural OM behavior, this model provides a much needed robust system for antibiotic development. Understanding the outer membranes of Gram‐negative bacteria is important for the development of new antibacterial compounds. However, their structure and dynamics are poorly understood because of their small in vivo size and inaccurate in vitro models. 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subjects Anti-Bacterial Agents - pharmacology
antibiotics
Bacterial Outer Membrane Proteins - chemistry
Communications
Drug Discovery
Drug Resistance, Bacterial
Escherichia coli - chemistry
Escherichia coli - cytology
Escherichia coli - drug effects
Escherichia coli Infections - drug therapy
Escherichia coli Infections - microbiology
Escherichia coli Proteins - chemistry
Gram-negative bacteria
Humans
Lipid Bilayers - chemistry
membranes
Membranes, Artificial
Models, Molecular
Phospholipids - chemistry
structure-activity relationships
title An Accurate In Vitro Model of the E. coli Envelope
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