4.6 Article

Cost-Effective Live Cell Structured Illumination Microscopy with Video-Rate Imaging

期刊

ACS PHOTONICS
卷 8, 期 6, 页码 1639-1648

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsphotonics.0c01937

关键词

structured illumination microscopy; digital micromirror devices; super-resolution; live cell imaging; video-rate imaging

资金

  1. Deutsche Forschungsgemeinschaft (DFG, German Science Foundation) [415832635]
  2. European Union [752080]
  3. Marie Curie Actions (MSCA) [752080] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

This paper presents a compact, cost-effective high-speed structured illumination microscope that allows for video-rate super-resolved image reconstructions. The instrument, based on a digital micromirror device and a global-shutter camera, optimizes SIM pattern contrast and enables real-time reconstruction and visualization of living cells with high sensitivity.
Optical nanoscopy is rapidly gaining momentum in the life sciences. Current instruments are, however, often large and expensive, and there is a substantial delay between raw data collection and super-resolved image display. Here, we describe the implementation of a compact, cost-effective, high-speed, structured illumination microscope (SIM), which allows for video-rate super-resolved image reconstructions at imaging rates up to 60 Hz. The instrument is based on a digital micromirror device (DMD) and a global-shutter camera, which enables faster pattern cycles and higher duty cycles than commonly used liquid crystal-based spatial light modulators. In order to utilize a DMD for creating illumination patterns by the coherent superposition of laser beams, we carefully studied its blazed grating effect Through both simulation and experimental determination of system parameters, we identified and optimized its alignment for optimal SIM pattern contrast. Raw image data are collected using inexpensive industry-grade CMOS cameras, while a parallel-computing platform allowed us to reconstruct and visualize living cells in real time. We demonstrate the performance of this system by imaging submicron-sized fluorescent beads diffusing in an aqueous solution, resolving bead-bead interactions in real time. We show that the system is sensitive enough to image intracellular vesicles labeled with fluorescent proteins in fixed cells. We also image dynamic fluctuations of the endoplasmic reticulum (ER), as well as the movement of mitochondria in living osteosarcoma cells, where the cellular organelles are labeled with live cell fluorescent stains.

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