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Int J Mol Sci. 2012 Nov 8;13(11):14545-64. doi: 10.3390/ijms131114545.
2
Fluorescence microspectroscopy as a tool to study mechanism of nanoparticles delivery into living cancer cells.荧光显微光谱法作为研究纳米颗粒递送至活癌细胞机制的工具。
Biomed Opt Express. 2011 Aug 1;2(8):2083-95. doi: 10.1364/BOE.2.2083. Epub 2011 Jun 29.
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Stable and unstable lipid domains in ceramide-containing membranes.含神经酰胺的膜中稳定和不稳定的脂质域。
Biophys J. 2011 May 4;100(9):2160-8. doi: 10.1016/j.bpj.2011.03.013.
4
Nitroxide-fluorophore double probes: a potential tool for studying membrane heterogeneity by ESR and fluorescence.氮氧自由基-荧光团双探针:通过电子自旋共振和荧光研究膜异质性的潜在工具。
Org Biomol Chem. 2011 Jun 7;9(11):4150-9. doi: 10.1039/c0ob01173h. Epub 2011 Apr 19.
5
Comparison of three ternary lipid bilayer mixtures: FRET and ESR reveal nanodomains.三种三元脂质双层混合物的比较:FRET 和 ESR 揭示纳米区。
Biophys J. 2010 Nov 17;99(10):3309-18. doi: 10.1016/j.bpj.2010.09.064.
6
Revitalizing membrane rafts: new tools and insights.振兴膜筏:新工具和新见解。
Nat Rev Mol Cell Biol. 2010 Oct;11(10):688-99. doi: 10.1038/nrm2977.
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Quantum efficiency independence of the time integrated emission from a fluorescent molecule.荧光分子的时间积分发射的量子效率独立性。
Appl Opt. 1976 Dec 1;15(12):3135-9. doi: 10.1364/AO.15.003135.
8
Surface topography of membrane domains.膜结构域的表面形貌。
Biochim Biophys Acta. 2010 Apr;1798(4):703-18. doi: 10.1016/j.bbamem.2009.09.015. Epub 2009 Sep 29.
9
Cholesterol-induced fluid membrane domains: a compendium of lipid-raft ternary phase diagrams.胆固醇诱导的流体膜结构域:脂质筏三元相图综述
Biochim Biophys Acta. 2009 Oct;1788(10):2114-23. doi: 10.1016/j.bbamem.2009.08.004. Epub 2009 Aug 21.
10
SDSL-ESR-based protein structure characterization.基于 SDSL-ESR 的蛋白质结构特征描述。
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脂质相中的探针构象共存——偏振荧光微光谱研究。

Coexistence of probe conformations in lipid phases-a polarized fluorescence microspectroscopy study.

机构信息

Laboratory of Biophysics, Condensed Matter Physics Department, Jožef Stefan Institute, Ljubljana, Slovenia.

出版信息

Biophys J. 2013 Aug 20;105(4):919-27. doi: 10.1016/j.bpj.2013.07.005.

DOI:10.1016/j.bpj.2013.07.005
PMID:23972844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3752113/
Abstract

Several well-established fluorescence methods depend on environment-sensitive probes that report about molecular properties of their local environment. For reliable interpretation of experiments, careful characterization of probes' behavior is required. In this study, bleaching-corrected polarized fluorescence microspectroscopy with nanometer spectral peak position resolution was applied to characterize conformations of two alkyl chain-labeled 7-nitro-2-1,3-benzoxadiazol-4-yl phospholipids in three model membranes, representing the three main lipid phases. The combination of polarized and spectral detection revealed two main probe conformations with their preferential fluorophore dipole orientations roughly parallel and perpendicular to membrane normal. Their peak positions were separated by 2-6 nm because of different local polarities and depended on lipid environment. The relative populations of conformations, estimated by a numerical model, indicated a specific sensitivity of the two probes to molecular packing with cholesterol. The coexistence of probe conformations could be further exploited to investigate membrane organization below microscopy spatial resolution, such as lipid rafts. With the addition of polarized excitation or detection to any environment-sensitive fluorescence imaging technique, the conformational analysis can be directly applied to explore local membrane complexity.

摘要

几种成熟的荧光方法依赖于环境敏感探针,这些探针可以报告其局部环境的分子特性。为了可靠地解释实验结果,需要仔细表征探针的行为。在这项研究中,采用漂白校正的偏振荧光显微光谱法,具有纳米光谱峰位置分辨率,用于表征两种烷基链标记的 7-硝基-2-1,3-苯并恶二唑-4-基磷脂在三种模型膜中的构象,这三种模型膜代表了三种主要的脂质相。偏振和光谱检测的结合揭示了两种主要的探针构象,其荧光团偶极子取向大致平行和垂直于膜法线。由于局部极性不同,它们的峰位置相差 2-6nm,并取决于脂质环境。通过数值模型估计的构象相对丰度表明,这两种探针对胆固醇的分子排列具有特定的敏感性。探针构象的共存可以进一步用于研究低于显微镜空间分辨率的膜组织,例如脂筏。通过向任何环境敏感的荧光成像技术添加偏振激发或检测,可以直接应用构象分析来探索局部膜的复杂性。