Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes

Naturally occurring linear polyamines are known to enable bacteria to be resistant to cationic membrane active peptides. To understand this protective mechanism, molecular dynamics simulations are employed to probe their effect on a model bacterial outer membrane. Being protonated at physiological p...

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Main Authors: Li, Jianguo, Beuerman, Roger, Verma, Chandra Shekhar
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/152155
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1521552021-09-13T08:52:51Z Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes Li, Jianguo Beuerman, Roger Verma, Chandra Shekhar School of Biological Sciences Bioinformatics Institute, A*STAR National University of Singapore Science::Biological sciences Molecular Dynamics Simulations Low Molecular Weight Linear Polyamine Naturally occurring linear polyamines are known to enable bacteria to be resistant to cationic membrane active peptides. To understand this protective mechanism, molecular dynamics simulations are employed to probe their effect on a model bacterial outer membrane. Being protonated at physiological pH, the amine groups of the polyamine engage in favorable electrostatic interactions with the negatively charged phosphate groups of the membrane. Additionally, the amine groups form large number of hydrogen bonds with the phosphate groups. At high concentrations, these hydrogen bonds and the electrostatic network can non-covalently crosslink the lipid A molecules, resulting in stabilization of the outer membrane against membrane active antibiotics such as colistin and polymyxin B. Moreover, large polyamine molecules (e.g., spermidine) have a stronger stabilization effect than small polyamine molecules (e.g., ethylene diamine). The atomistic insights provide useful guidance for the design of next generation membrane active amine-rich antibiotics, especially to tackle the growing threat of multi-drug resistance of Gram negative bacteria. National Medical Research Council (NMRC) This work was supported by NMRC/TCR/002-SERI/2008/ R618, NMRC/TCR/R1018. 2021-09-13T08:52:51Z 2021-09-13T08:52:51Z 2020 Journal Article Li, J., Beuerman, R. & Verma, C. S. (2020). Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes. Biochimica et Biophysica Acta - Biomembranes, 1862(9), 183297-. https://dx.doi.org/10.1016/j.bbamem.2020.183297 0005-2728 https://hdl.handle.net/10356/152155 10.1016/j.bbamem.2020.183297 32339485 2-s2.0-85084521637 9 1862 183297 en NMRC/TCR/002-SERI/2008/ R618 NMRC/TCR/R1018 Biochimica et Biophysica Acta - Biomembranes © 2020 Elsevier B.V. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
Molecular Dynamics Simulations
Low Molecular Weight Linear Polyamine
spellingShingle Science::Biological sciences
Molecular Dynamics Simulations
Low Molecular Weight Linear Polyamine
Li, Jianguo
Beuerman, Roger
Verma, Chandra Shekhar
Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
description Naturally occurring linear polyamines are known to enable bacteria to be resistant to cationic membrane active peptides. To understand this protective mechanism, molecular dynamics simulations are employed to probe their effect on a model bacterial outer membrane. Being protonated at physiological pH, the amine groups of the polyamine engage in favorable electrostatic interactions with the negatively charged phosphate groups of the membrane. Additionally, the amine groups form large number of hydrogen bonds with the phosphate groups. At high concentrations, these hydrogen bonds and the electrostatic network can non-covalently crosslink the lipid A molecules, resulting in stabilization of the outer membrane against membrane active antibiotics such as colistin and polymyxin B. Moreover, large polyamine molecules (e.g., spermidine) have a stronger stabilization effect than small polyamine molecules (e.g., ethylene diamine). The atomistic insights provide useful guidance for the design of next generation membrane active amine-rich antibiotics, especially to tackle the growing threat of multi-drug resistance of Gram negative bacteria.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Li, Jianguo
Beuerman, Roger
Verma, Chandra Shekhar
format Article
author Li, Jianguo
Beuerman, Roger
Verma, Chandra Shekhar
author_sort Li, Jianguo
title Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
title_short Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
title_full Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
title_fullStr Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
title_full_unstemmed Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
title_sort mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes
publishDate 2021
url https://hdl.handle.net/10356/152155
_version_ 1712300626112675840