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荧光各向异性再装填——用于评估单分子、颗粒、薄膜及其他体系中发色团组织和激发能量转移的新兴偏振显微镜方法

Fluorescence Anisotropy Reloaded-Emerging Polarization Microscopy Methods for Assessing Chromophores' Organization and Excitation Energy Transfer in Single Molecules, Particles, Films, and Beyond.

作者信息

Camacho Rafael, Täuber Daniela, Scheblykin Ivan G

机构信息

Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001, Leuven, Belgium.

Chemical Physics and NanoLund, Lund University, P.O. Box 124, SE-22100, Lund, Sweden.

出版信息

Adv Mater. 2019 May;31(22):e1805671. doi: 10.1002/adma.201805671. Epub 2019 Feb 5.

DOI:10.1002/adma.201805671
PMID:30721532
Abstract

Fluorescence polarization is widely used to assess the orientation/rotation of molecules, and the excitation energy transfer between closely located chromophores. Emerging since the 1990s, single molecule fluorescence spectroscopy and imaging stimulate the application of light polarization for studying molecular organization and energy transfer beyond ensemble averaging. Here, traditional fluorescence polarization and linear dichroism methods used for bulk samples are compared with techniques specially developed for, or inspired by, single molecule fluorescence spectroscopy. Techniques for assessing energy transfer in anisotropic samples, where the traditional fluorescence anisotropy framework is not readily applicable, are discussed in depth. It is shown that the concept of a polarization portrait and the single funnel approximation can lay the foundation for alternative energy transfer metrics. Examples ranging from fundamental studies of photoactive materials (conjugated polymers, light-harvesting aggregates, and perovskite semiconductors) to Förster resonant energy transfer (FRET)-based biomedical imaging are presented. Furthermore, novel uses of light polarization for super-resolution optical imaging are mentioned as well as strategies for avoiding artifacts in polarization microscopy.

摘要

荧光偏振被广泛用于评估分子的取向/旋转以及紧密相邻发色团之间的激发能量转移。自20世纪90年代以来出现的单分子荧光光谱和成像技术,推动了光偏振在研究分子组织和超越系综平均的能量转移方面的应用。在此,将用于块状样品的传统荧光偏振和线性二向色性方法与专门为单分子荧光光谱开发或受其启发而发展的技术进行比较。深入讨论了在传统荧光各向异性框架不易适用的各向异性样品中评估能量转移的技术。结果表明,偏振图谱概念和单漏斗近似可为替代能量转移度量奠定基础。展示了从光活性材料(共轭聚合物、光捕获聚集体和钙钛矿半导体)的基础研究到基于Förster共振能量转移(FRET)的生物医学成像等示例。此外,还提到了光偏振在超分辨率光学成像中的新用途以及避免偏振显微镜中伪像的策略。

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