Jensen Ellen, Crossman David J
Anat Rec (Hoboken). 2014 Dec;297(12):2227-31. doi: 10.1002/ar.22960. Epub 2014 Jul 4.
In the 1990s, new concepts of microscopy revolutionized the imaging field by breaking the lateral resolution diffraction limit for the first time, even with propagating light and regular lenses (i.e., far-field). In 2006, several research groups independently showed super-resolution microscopy using high-precision localization of single fluorophores. These new developments in single-molecule spectroscopy enabled a different approach to achieving nanometer-scale optical microscopy. Direct stochastic optical reconstruction microscopy (dSTORM) is a technique of single-molecule super-resolution imaging that does not require an activator fluorophore. This technique is used to visualize cellular structures with a resolution of approximately 20 nm. dSTORM is compatible with many conventionally used fluorophores. This article provides an overview of the principles and uses of dSTORM. Advantages and disadvantages of dSTORM are also discussed.
20世纪90年代,显微镜学的新概念首次突破了横向分辨率衍射极限,彻底改变了成像领域,即便使用的是传播光和常规透镜(即远场)。2006年,几个研究小组独立展示了利用单个荧光团的高精度定位实现超分辨率显微镜技术。单分子光谱学的这些新进展为实现纳米级光学显微镜提供了一种不同的方法。直接随机光学重建显微镜(dSTORM)是一种单分子超分辨率成像技术,不需要激活荧光团。该技术用于以约20纳米的分辨率可视化细胞结构。dSTORM与许多传统使用的荧光团兼容。本文概述了dSTORM的原理和用途。还讨论了dSTORM的优缺点。