The intricate link between membrane lipid structure and composition and membrane structural properties in bacterial membranes

被引:31
作者
Lee, Tzong-Hsien [1 ]
Charchar, Patrick [2 ]
Separovic, Frances [3 ]
Reid, Gavin E. [3 ,4 ]
Yarovsky, Irene [2 ]
Aguilar, Marie-Isabel [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[2] RMIT Univ, Sch Engn, Melbourne, Vic 3001, Australia
[3] Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Sch Chem, Melbourne, Vic 3010, Australia
[4] Univ Melbourne, Dept Biochem & Pharmacol, Parkville, Vic 3010, Australia
基金
英国医学研究理事会;
关键词
ATOMIC-FORCE MICROSCOPY; UNSATURATED FATTY-ACIDS; ANTIMICROBIAL PEPTIDE RESISTANCE; CLASS IIA BACTERIOCIN; ESCHERICHIA-COLI; STAPHYLOCOCCUS-AUREUS; MODEL MEMBRANES; OUTER-MEMBRANE; PHOSPHOLIPID-COMPOSITION; ELECTRON-MICROSCOPY;
D O I
10.1039/d3sc04523d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is now evident that the cell manipulates lipid composition to regulate different processes such as membrane protein insertion, assembly and function. Moreover, changes in membrane structure and properties, lipid homeostasis during growth and differentiation with associated changes in cell size and shape, and responses to external stress have been related to drug resistance across mammalian species and a range of microorganisms. While it is well known that the biomembrane is a fluid self-assembled nanostructure, the link between the lipid components and the structural properties of the lipid bilayer are not well understood. This perspective aims to address this topic with a view to a more detailed understanding of the factors that regulate bilayer structure and flexibility. We describe a selection of recent studies that address the dynamic nature of bacterial lipid diversity and membrane properties in response to stress conditions. This emerging area has important implications for a broad range of cellular processes and may open new avenues of drug design for selective cell targeting. The dynamic nature of bacterial lipid diversity and membrane properties in response to stress conditions is discussed. This emerging area has implications for a range of cellular processes and drug design for selective cell targeting.
引用
收藏
页码:3408 / 3427
页数:20
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