Department of Human Protein Sciences, University of Geneva, CMU, Genève 4, Switzerland.
Phys Chem Chem Phys. 2013 Sep 28;15(36):14919-30. doi: 10.1039/c3cp52289j.
Fluorescence imaging beyond the diffraction limit has grown into a method of choice to elucidate questions related to biological structure and organisation. Among super-resolution techniques, imaging based on the localization of individual photoswitchable fluorescent probes has become particularly popular due to its relative ease of implementation and the nature of qualitative and quantitative answers it can offer. We review the field of single-molecule localization microscopy (SMLM) by providing an overview of its underlying principles and of different categories of photoswitchable fluorophores. In addition to summarizing target-specific labelling strategies and presenting examples of successful applications of SMLM in fixed and living systems, we show how SMLM data offer unique opportunities for quantitative biomolecular counting and distribution analysis.
荧光成像是一种超越衍射极限的方法,已经成为阐明与生物结构和组织相关问题的首选方法。在超分辨率技术中,基于单个光可开关荧光探针定位的成像技术由于其相对简单的实现方式以及可以提供定性和定量答案的性质而变得特别受欢迎。我们通过概述其基本原理和不同类别的光可开关荧光染料,来回顾单分子定位显微镜(SMLM)领域。除了总结针对特定目标的标记策略并展示 SMLM 在固定和活细胞系统中的成功应用实例外,我们还展示了 SMLM 数据如何为定量生物分子计数和分布分析提供独特的机会。