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脂质网络。

The lipid network.

作者信息

Sani Marc-Antoine, Separovic Frances, Gehman John D

机构信息

School of Chemistry, Bio21 Institute, University of Melbourne, Melbourne, VIC, 3010, Australia.

出版信息

Biophys Rev. 2012 Dec;4(4):283-290. doi: 10.1007/s12551-012-0071-1. Epub 2012 Mar 24.

DOI:10.1007/s12551-012-0071-1
PMID:28510205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5430237/
Abstract

Natural cell membranes are composed of a remarkable variety of lipids, which provide specific biophysical properties to support membrane protein function. An improved understanding of this complexity of membrane composition may also allow the design of membrane active drugs. Crafting a relevant model of a cell membrane with controlled composition is becoming an art, with the ability to reveal the molecular mechanisms of biological processes and lead to better treatment of pathologies. By matching physiological observations from in vivo experiments to high-resolution information, more easily obtained from in vitro studies, complex interactions at the lipid interface are determined. The role of the lipid network in biological membranes is, therefore, the subject of increasing attention.

摘要

天然细胞膜由种类繁多的脂质组成,这些脂质提供特定的生物物理特性以支持膜蛋白的功能。对膜成分这种复杂性的深入理解也可能有助于设计膜活性药物。构建具有可控成分的相关细胞膜模型正成为一门艺术,它能够揭示生物过程的分子机制并带来更好的疾病治疗方法。通过将体内实验的生理学观察结果与更容易从体外研究中获得的高分辨率信息相匹配,可以确定脂质界面处的复杂相互作用。因此,脂质网络在生物膜中的作用越来越受到关注。

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本文引用的文献

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In-cell NMR spectroscopy.细胞内核磁共振光谱法。
Prog Nucl Magn Reson Spectrosc. 2011 Oct;59(3):197-212. doi: 10.1016/j.pnmrs.2010.11.002. Epub 2010 Nov 17.
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Direct observation of single amyloid-β(1-40) oligomers on live cells: binding and growth at physiological concentrations.直接观察活细胞上的单个淀粉样β(1-40)寡聚物:在生理浓度下的结合和生长。
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In situ structural characterization of a recombinant protein in native Escherichia coli membranes with solid-state magic-angle-spinning NMR.利用固态魔角旋转 NMR 对天然大肠杆菌膜中的重组蛋白进行原位结构表征。
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Solid-state NMR of amyloid membrane interactions.淀粉样蛋白与膜相互作用的固态核磁共振研究
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Persistence of antibiotic resistance in bacterial populations.细菌种群中抗生素耐药性的持续存在。
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Antibiotic activities of host defense peptides: more to it than lipid bilayer perturbation.宿主防御肽的抗生素活性:远不止于脂质双层扰动。
Nat Prod Rep. 2011 Aug;28(8):1350-8. doi: 10.1039/c1np00022e. Epub 2011 May 27.
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Bacterial resistance mechanisms against host defense peptides.细菌对抗宿主防御肽的耐药机制。
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