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通过荧光光谱和显微镜技术跟踪细胞膜流动性的全局和局部变化。

Tracking Global and Local Changes in Membrane Fluidity Through Fluorescence Spectroscopy and Microscopy.

机构信息

Centre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK.

Division of Chemical Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

出版信息

Methods Mol Biol. 2023;2601:203-229. doi: 10.1007/978-1-0716-2855-3_11.

Abstract

Membrane fluidity is a critical parameter of cellular membranes, which cells continuously strive to maintain within a viable range. Interference with the correct membrane fluidity state can strongly inhibit cell function. Triggered changes in membrane fluidity and associated impacts on lipid domains have been postulated to contribute to the mechanism of action of membrane targeting antimicrobials, but the corresponding analyses have been hampered by the absence of readily available analytical tools. Here, we expand upon the protocols outlined in the first edition of this book, providing further and alternative protocols that can be used to measure changes in membrane fluidity. We provide detailed protocols, which allow straightforward in vivo and in vitro measurement of antibiotic compound-triggered changes in membrane fluidity and fluid membrane microdomains. Furthermore, we summarize useful strains constructed by us and others to characterize and confirm lipid specificity of membrane antimicrobials directly in vivo.

摘要

膜流动性是细胞膜的一个关键参数,细胞会不断努力将其维持在一个可行的范围内。干扰正确的膜流动性状态会强烈抑制细胞功能。已经提出,膜流动性的触发变化以及对脂质域的相关影响有助于膜靶向抗菌药物的作用机制,但由于缺乏现成的分析工具,相应的分析受到了阻碍。在这里,我们扩展了本书第一版中概述的方案,提供了进一步和替代的方案,可用于测量膜流动性的变化。我们提供了详细的方案,允许在体内和体外轻松测量抗生素化合物触发的膜流动性和流动膜微区的变化。此外,我们总结了我们和其他人构建的有用菌株,以直接在体内表征和确认膜抗菌剂的脂质特异性。

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