Fernández-Suárez Marta, Ting Alice Y
Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
Nat Rev Mol Cell Biol. 2008 Dec;9(12):929-43. doi: 10.1038/nrm2531. Epub 2008 Nov 12.
In 1873, Ernst Abbe discovered that features closer than approximately 200 nm cannot be resolved by lens-based light microscopy. In recent years, however, several new far-field super-resolution imaging techniques have broken this diffraction limit, producing, for example, video-rate movies of synaptic vesicles in living neurons with 62 nm spatial resolution. Current research is focused on further improving spatial resolution in an effort to reach the goal of video-rate imaging of live cells with molecular (1-5 nm) resolution. Here, we describe the contributions of fluorescent probes to far-field super-resolution imaging, focusing on fluorescent proteins and organic small-molecule fluorophores. We describe the features of existing super-resolution fluorophores and highlight areas of importance for future research and development.
1873年,恩斯特·阿贝发现,基于透镜的光学显微镜无法分辨间距小于约200纳米的特征。然而,近年来,几种新的远场超分辨率成像技术突破了这一衍射极限,例如,以62纳米的空间分辨率拍摄了活神经元中突触小泡的视频速率影片。当前的研究集中在进一步提高空间分辨率,以期实现对活细胞进行分子(1 - 5纳米)分辨率的视频速率成像这一目标。在此,我们描述荧光探针在远场超分辨率成像中的作用,重点介绍荧光蛋白和有机小分子荧光团。我们阐述了现有超分辨率荧光团的特性,并突出了未来研发的重要领域。