SRRF: Universal live-cell super-resolution microscopy

被引:121
作者
Culley, Sian [1 ,2 ,3 ]
Tosheva, Kalina L. [1 ,2 ]
Pereira, Pedro Matos [1 ,2 ,3 ]
Henriques, Ricardo [1 ,2 ,3 ]
机构
[1] UCL, MRC Lab Mol Cell Biol, Gower St, London WC1E 6BT, England
[2] UCL, Dept Cell & Dev Biol, Gower St, London WC1E 6BT, England
[3] Francis Crick Inst, 1 Midland Rd, London NW1 1AT, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Super-resolution microscopy; Fluorescence; Image processing; Live-cell imaging; STRUCTURED-ILLUMINATION MICROSCOPY; SUBDIFFRACTION-RESOLUTION; FLUORESCENCE MICROSCOPY; LOCALIZATION; NANOSCOPY; PROBES; STORM; LIMIT;
D O I
10.1016/j.biocel.2018.05.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Super-resolution microscopy techniques break the diffraction limit of conventional optical microscopy to achieve resolutions approaching tens of nanometres. The major advantage of such techniques is that they provide resolutions close to those obtainable with electron microscopy while maintaining the benefits of light microscopy such as a wide palette of high specificity molecular labels, straightforward sample preparation and live-cell compatibility. Despite this, the application of super-resolution microscopy to dynamic, living samples has thus far been limited and often requires specialised, complex hardware. Here we demonstrate how a novel analytical approach, Super-Resolution Radial Fluctuations (SRRF), is able to make live-cell super-resolution microscopy accessible to a wider range of researchers. We show its applicability to live samples expressing GFP using commercial confocal as well as laser- and LED-based widefield microscopes, with the latter achieving long-term timelapse imaging with minimal photobleaching.
引用
收藏
页码:74 / 79
页数:6
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