Fast structured illumination microscopy using rolling shutter cameras

被引:29
|
作者
Song, Liyan [1 ,2 ]
Lu-Walther, Hui-Wen [1 ]
Foester, Ronny [1 ,3 ]
Jost, Aurelie [1 ,3 ]
Kielhorn, Martin [1 ,3 ,5 ]
Zhou, Jianying [2 ,4 ]
Heintzmann, Rainer [1 ,3 ]
机构
[1] Leibniz Inst Photon Technol, Jena, Germany
[2] Sun Yat Sen Univ, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Guangdong, Peoples R China
[3] Univ Jena, Inst Phys Chem, Abbe Ctr Photon, Jena, Germany
[4] SYSU CMU Shunde Int Joint Res Inst, Shunde 528300, Peoples R China
[5] eZono AG, D-07743 Jena, Germany
关键词
structured illumination microscopy; superresolution; video rate; spatial light modulators; synchronization; STED NANOSCOPY; EXCITATION MICROSCOPY; STIMULATED-EMISSION; RESOLUTION LIMIT; LIVING CELL; LIVE CELLS; IMPROVEMENT; REVEALS;
D O I
10.1088/0957-0233/27/5/055401
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Spatial light modulators (SLM) update in a synchronous manner, whereas the data readout process in fast structured illumination systems is usually done using a rolling shutter camera with asynchronous readout. In structured illumination microscopy (SIM), this leads to synchronization problems causing a speed limit for fast acquisition. In this paper we present a configuration to overcome this limit by exploiting the extremely fast SLM display and dividing it into several segments along the direction of the rolling shutter of the sCMOS camera and displaying multiple SLM frames per camera acquisition. The sCMOS runs in continuous rolling shutter mode and the SLM keeps the readout-line always inside a dark region presenting different SIM patterns before and after the readout/start-exposure line. Using this approach, we reached a raw frame rate of 714 frames per second (fps) resulting in a two-beam SIM acquisition rate of 79 fps with a region of interest (ROI) of 16.5 x 16.5 mu m(2).
引用
收藏
页数:6
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