Finan Kieran, Flottmann Benjamin, Heilemann Mike
Department of Biotechnology and Biophysics, Julius-Maximilians University Würzburg, Würzburg, Germany.
Methods Mol Biol. 2013;950:131-51. doi: 10.1007/978-1-62703-137-0_9.
Over the past decade, fluorescence microscopy has been revolutionized by the development of novel techniques that allow near-molecular resolution. Many such methods-collectively referred to as "single-molecule localization microscopy" (SMLM)-are based upon the repeated imaging of sparse stochastic subsets of the fluorophores in a sample. Active fluorophores are localized by finding the centers of their point spread functions, and a super-resolution image is constructed.Key to this strategy is the use of fluorophores that can be switched "on" and "off" in a controllable manner. Here we review the strengths and weaknesses of the wide variety of SMLM-compatible photoswitchable fluorophores and labeling strategies currently available. We also discuss their suitability for live-cell and multicolor imaging, as well as molecular counting.
在过去十年中,荧光显微镜技术因能够实现近分子分辨率的新技术的发展而发生了变革。许多此类方法——统称为“单分子定位显微镜”(SMLM)——基于对样品中荧光团稀疏随机子集的重复成像。通过找到活性荧光团的点扩散函数中心来对其进行定位,进而构建超分辨率图像。该策略的关键在于使用能够以可控方式“开启”和“关闭”的荧光团。在此,我们综述了目前可用的各种与SMLM兼容的光开关荧光团和标记策略的优缺点。我们还讨论了它们在活细胞成像、多色成像以及分子计数方面的适用性。