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LED Thermo Flow - Combining Optogenetics with Flow Cytometry

MPS-Authors

Brenker,  Kathrin
Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;
Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg;
Centre for Biological Signaling Studies, BIOSS, University of Freiburg;

Osthof,  Kerstin
Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;
Albert-Ludwigs-Universität;

Yang,  Jianying
Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;
Centre for Biological Signaling Studies, BIOSS, University of Freiburg;

Reth ,  Michael
Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;
Centre for Biological Signaling Studies, BIOSS, University of Freiburg;
Insitute of Biology III (Mol. Immunology), Albert-Ludwigs-Universität;

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Citation

Brenker, K., Osthof, K., Yang, J., & Reth, M. (2016). LED Thermo Flow - Combining Optogenetics with Flow Cytometry. Journal of visualized experiments, 118, e54707-e54707. doi:10.3791/54707.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002C-A8CB-8
Abstract
Optogenetic tools allow isolated, functional investigations of almost any signaling molecule within complex signaling pathways. A major obstacle is the controlled delivery of light to the cell sample and hence the most popular tools for optogenetic studies are microscopy-based cell analyses and in vitro experiments. The flow cytometer has major advantages over a microscope, including the ability to rapidly measure thousands of cells at single cell resolution. However, it is not yet widely used in optogenetics. Here, we present a device that combines the power of optogenetics and flow cytometry: the LED Thermo Flow. This device illuminates cells at specific wavelengths, light intensities and temperatures during flow cytometric measurements. It can be built at low cost and be used with most common flow cytometers. To demonstrate its utility, we characterized the photoswitching kinetics of Dronpa proteins in vivo and in real time. This protocol can be adapted to almost all optically controlled substances and substantially expands the set of possible experiments. More importantly, it will greatly simplify the discovery and development of new optogenetic tools.