Fluorescent markers in microscopy: photophysical characteristics and applications in cell biology

Urban Bogataj, J. Štrus, N. Žnidaršič, M. Kreft
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引用次数: 0

Abstract

In the fluorescence microscopy of biological specimens the structures in cells and tissues usually need to be labelled with various fluorescent markers. The three main groups of fluorescent markers are small organic fluorochromes, fluorescent proteins and quantum dots. Fluorescent markers differ according to photophysical properties and binding specificity for the selected target structures in the sample. For the labelling of specific structures with small organic fluorochromes or quantum dots it is usually necessary to conjugate them with target-specific macromolecules. For the labelling with fluorescent proteins it is necessary to introduce a fluorescent protein gene into the observed cells or organism. The most important photophysical properties of fluorescent markers are absorption and emission spectra, Stokes shift, extinction coefficient and quantum yield. Currently, various super-resolution fluorescent microscopy techniques exploit special fluorochromes that enable fluorescence modulation by specific wavelength illumination, to achieve the resolution below the diffraction limit.
显微荧光标记物:光物理特性及其在细胞生物学中的应用
在生物标本的荧光显微镜中,通常需要用各种荧光标记来标记细胞和组织的结构。三种主要的荧光标记是小有机荧光染料、荧光蛋白和量子点。荧光标记根据样品中所选目标结构的光物理性质和结合特异性而有所不同。为了用小有机荧光染料或量子点标记特定结构,通常需要将它们与目标特异性大分子偶联。为了用荧光蛋白进行标记,必须将荧光蛋白基因引入观察到的细胞或生物体中。荧光标记物最重要的光物理性质是吸收和发射光谱、斯托克斯位移、消光系数和量子产率。目前,各种超分辨率荧光显微镜技术利用特殊的荧光染料,通过特定波长的照明来实现荧光调制,以达到低于衍射极限的分辨率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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