| Literature DB >> 29693956 |
Youhua Chen1,2, Ruizhi Cao1, Wenjie Liu1, Dazhao Zhu1, Zhiming Zhang1, Cuifang Kuang1,3, Xu Liu1,3.
Abstract
We present an alternative approach to realize structured illumination microscopy (SIM), which is capable for live cell imaging. The prototype utilizes two sets of scanning galvo mirrors, a polarization converter and a piezo-platform to generate a fast shifted, s-polarization interfered and periodic variable illumination patterns. By changing the angle of the scanning galvanometer, we can change the position of the spots at the pupil plane of the objective lens arbitrarily, making it easy to switch between widefield and total internal reflection fluorescent-SIM mode and adapting the penetration depth in the sample. Also, a twofold resolution improvement is achieved in our experiments. The prototype offers more flexibility of pattern period and illumination orientation changing than previous systems. (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE).Keywords: fluorescence microscopy; scanning galvo mirrors; structure illumination; super-resolution; total internal reflection
Mesh:
Year: 2018 PMID: 29693956 DOI: 10.1117/1.JBO.23.4.046007
Source DB: PubMed Journal: J Biomed Opt ISSN: 1083-3668 Impact factor: 3.170