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Time-Resolved Fluorescence in Lipid Bilayers: Selected Applications and Advantages over Steady State

机译:脂质双层中的时间分辨荧光:稳态的某些应用和优势

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摘要

Fluorescence methods are versatile tools for obtaining dynamic and topological information about biomembranes because the molecular interactions taking place in lipid membranes frequently occur on the same timescale as fluorescence emission. The fluorescence intensity decay, in particular, is a powerful reporter of the molecular environment of a fluorophore. The fluorescence lifetime can be sensitive to the local polarity, hydration, viscosity, and/or presence of fluorescence quenchers/energy acceptors within several nanometers of the vicinity of a fluorophore. Illustrative examples of how time-resolved fluorescence measurements can provide more valuable and detailed information about a system than the time-integrated (steady-state) approach will be presented in this review: 1), determination of membrane polarity and mobility using time-dependent spectral shifts; 2), identification of submicroscopic domains by fluorescence lifetime imaging microscopy; 3), elucidation of membrane leakage mechanisms from dye self-quenching assays; and 4), evaluation of nanodomain sizes by time-resolved Förster resonance energy transfer measurements.
机译:荧光方法是获取生物膜动态和拓扑信息的通用工具,因为脂质膜中发生的分子相互作用通常在与荧光发射相同的时间尺度上发生。荧光强度的衰减尤其是荧光团分子环境的有力报道。荧光寿命可以对荧光团附近几纳米内的局部极性,水合,粘度和/或荧光猝灭剂/能量受体的存在敏感。与时间积分(稳态)方法相比,时间分辨荧光测量如何提供有关系统的更多有价值和详细信息的说明性示例将在本综述中提供:1),使用时间相关的膜极性和迁移率测定光谱位移2),通过荧光寿命成像显微镜鉴定亚显微区域; 3)从染料自猝灭分析中阐明膜泄漏的机理;和4),通过时间分辨的Förster共振能量转移测量评估纳米域尺寸。

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