Live TIRF fluorescence imaging at 100nm resolution through structured illumination

被引:3
作者
Kner, P. [1 ,2 ]
Chhun, B. [2 ]
Griffis, E. [2 ]
Winoto, L. [2 ]
Shao, L. [2 ]
Gustafsson, M. G. L. [2 ]
机构
[1] Univ Georgia, Fac Engn, Driftmier Engn Ctr, Athens, GA 30602 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
来源
THREE-DIMENSIONAL AND MULTIDIMENSIONAL MICROSCOPY: IMAGE ACQUISITION AND PROCESSING XVI | 2009年 / 7184卷
基金
美国国家科学基金会;
关键词
Structured illumination; Super-resolution; Microscopy; Bio-imaging; MICROSCOPY; DYNAMICS; PROTEIN; LIMIT;
D O I
10.1117/12.812351
中图分类号
TH742 [显微镜];
学科分类号
摘要
Linear Structured Illumination is a powerful technique for increasing the resolution of a fluorescence microscope by a factor of two beyond the diffraction limit. Previously this technique has only been used to image fixed samples because the implementation, using a mechanically rotated fused silica grating, was too slow. Here we describe a microscope design, using a ferroelectric spatial light modulator to structure the illumination light, capable of linear structured illumination at frame rates up to 11Hz. We show live imaging of GFP labeled Tubulin and Kinesin in Drosophila S2 cells.
引用
收藏
页数:9
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